Methods and compositions for treating hepatitis c virus

ABSTRACT

A method and composition for treating a host infected with hepatitis C comprising administering an effective hepatitis C treatment amount of a described 1′, 2′ or 3′-modified nucleoside or a pharmaceutically acceptable salt or prodrug thereof, is provided.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 13/623,674, filed on Sep. 20, 2012, which is a continuation of U.S. application Ser. No. 12/504,601, filed on Jul. 16, 2009, which is a continuation of U.S. application Ser. No. 10/602,691, filed on Jun. 20, 2003, which is a continuation of U.S. application Ser. No. 09/864,078, filed on May 23, 2001, which claims the benefit of priority to U.S. Provisional Application No. 60/206,585, filed on May 23, 2000, the disclosure of each of which is incorporated herein by reference in its entirety.

FIELD OF THE INVENTION

This invention is in the area of pharmaceutical chemistry, and is in particular, is a compound, method and composition for the treatment of hepatitis C virus.

BACKGROUND OF THE INVENTION

The hepatitis C virus (HCV) is the leading cause of chronic liver disease worldwide. (Boyer, N. et al. J. Hepatol. 32:98-112, 2000). HCV causes a slow growing viral infection and is the major cause of cirrhosis and hepatocellular carcinoma (Di Besceglie, A. M. and Bacon, B. R., Scientific American, October: 80-85, (1999); Boyer, N. et al. J. Hepatol. 32:98-112, 2000). An estimated 170 million persons are infected with HCV worldwide. (Boyer, N. et al. J. Hepatol. 32:98-112, 2000). Cirrhosis caused by chronic hepatitis C infection accounts for 8,000-12,000 deaths per year in the United States, and HCV infection is the leading indication for liver transplant.

HCV is known to cause at least 80% of posttransfusion hepatitis and a substantial proportion of sporadic acute hepatitis. Preliminary evidence also implicates HCV in many cases of “idiopathic” chronic hepatitis, “cryptogenic” cirrhosis, and probably hepatocellular carcinoma unrelated to other hepatitis viruses, such as Hepatitis B Virus (HBV). A small proportion of healthy persons appear to be chronic HCV carriers, varying with geography and other epidemiological factors. The numbers may substantially exceed those for HBV, though information is still preliminary; how many of these persons have subclinical chronic liver disease is unclear. (The Merck Manual, ch. 69, p. 901, 16th ed., (1992)).

HCV has been classified as a member of the virus family Flaviviridae that includes the genera flaviviruses, pestiviruses, and hapaceiviruses which includes hepatitis C viruses (Rice, C. M., Flaviviridae: The viruses and their replication. In: Fields Virology, Editors: Fields, B. N., Knipe, D. M., and Howley, P. M., Lippincott-Raven Publishers, Philadelphia, Pa., Chapter 30, 931-959, 1996). HCV is an enveloped virus containing a positive-sense single-stranded RNA genome of approximately 9.4 kb. The viral genome consists of a 5′ untranslated region (UTR), a long open reading frame encoding a polyprotein precursor of approximately 3011 amino acids, and a short 3′ UTR. The 5′ UTR is the most highly conserved part of the HCV genome and is important for the initiation and control of polyprotein translation. Translation of the HCV genome is initiated by a cap-independent mechanism known as internal ribosome entry. This mechanism involves the binding of ribosomes to an RNA sequence known as the internal ribosome entry site (IRES). An RNA pseudoknot structure has recently been determined to be an essential structural element of the HCV IRES. Viral structural proteins include a nucleocapsid core protein (C) and two envelope glycoproteins, E1 and E2. HCV also encodes two proteinases, a zinc-dependent metalloproteinase encoded by the NS2-NS3 region and a serine proteinase encoded in the NS3 region. These proteinases are required for cleavage of specific regions of the precursor polyprotein into mature peptides. The carboxyl half of nonstructural protein 5, NS5B, contains the RNA-dependent RNA polymerase. The function of the remaining nonstructural proteins, NS4A and NS4B, and that of NS5A (the amino-terminal half of nonstructural protein 5) remain unknown.

A significant focus of current antiviral research is directed toward the development of improved methods of treatment of chronic HCV infections in humans (Di Besceglie, A. M. and Bacon, B. R., Scientific American, October: 80-85, (1999)). Currently, there are two primary antiviral compounds, Ribavirin and interferon-alpha, which are used for the treatment of chronic HCV infections in humans.

Treatment of HCV Infection with Ribivarin

Ribavirin (1-β-D-ribofuranosyl-1-1,2,4-triazole-3-carboxamide) is a synthetic, non-interferon-inducing, broad spectrum antiviral nucleoside analog sold under the trade name, Virazole (The Merck Index, 11th edition, Editor: Budavari, S., Merck & Co., Inc., Rahway, N.J., p1304, 1989). U.S. Pat. No. 3,798,209 and RE29,835 disclose and claim Ribavirin. Ribavirin is structurally similar to guanosine, and has in vitro activity against several DNA and RNA viruses including Flaviviridae (Gary L. Davis. Gastroenterology 118:S104-S114, 2000).

Ribavirin reduces serum amino transferase levels to normal in 40% or patients, but it does not lower serum levels of HCV-RNA (Gary L. Davis. Gastroenterology 118:S104-S114, 2000). Thus, Ribavirin alone is not effective in reducing viral RNA levels. Additionally, Ribavirin has significant toxicity and is known to induce anemia.

Treatment of HCV Infection with Interferon

Interferons (IFNs) are compounds that have been commercially available for the treatment of chronic hepatitis for nearly a decade. IFNs are glycoproteins produced by immune cells in response to viral infection. IFNs inhibit viral replication of many viruses, including HCV, and when used as the sole treatment for hepatitis C infection, IFN suppresses serum HCV-RNA to undetectable levels. Additionally, IFN normalizes serum amino transferase levels. Unfortunately, the effects of IFN are temporary and a sustained response occurs in only 8%-9% of patients chronically infected with HCV (Gary L. Davis. Gastroenterology 118:S104-S114, 2000).

A number of patents disclose HCV treatments using interferon-based therapies. For example, U.S. Pat. No. 5,980,884 to Blatt et al. discloses methods for retreatment of patients afflicted with HCV using consensus interferon. U.S. Pat. No. 5,942,223 to Bazer et al. discloses an anti-HCV therapy using ovine or bovine interferon-tau. U.S. Pat. No. 5,928,636 to Alber et al. discloses the combination therapy of interleukin-12 and interferon alpha for the treatment of infectious diseases including HCV. U.S. Pat. No. 5,908,621 to Glue et al. discloses the use of polyethylene glycol modified interferon for the treatment of HCV. U.S. Pat. No. 5,849,696 to Chretien et al. discloses the use of thymosins, alone or in combination with interferon, for treating HCV. U.S. Pat. No. 5,830,455 to Valtuena et al. discloses a combination HCV therapy employing interferon and a free radical scavenger. U.S. Pat. No. 5,738,845 to Imakawa discloses the use of human interferon tau proteins for treating HCV. Other interferon-based treatments for HCV are disclosed in U.S. Pat. No. 5,676,942 to Testa et al., U.S. Pat. No. 5,372,808 to Blatt et al., and U.S. Pat. No. 5,849,696.

Combination of Interferon and Ribavirin

The combination of IFN and Ribavirin for the treatment of HCV infection has been reported to be effective in the treatment of IFN naïve patients (Battaglia, A. M. et al., Ann. Pharmacother. 34:487-494, 2000). Results are promising for this combination treatment both before hepatitis develops or when histological disease is present (Berenguer, M. et al. Antivir. Ther. 3(Suppl. 3):125-136, 1998). Side effects of combination therapy include hemolysis, flu-like symptoms, anemia, and fatigue. (Gary L. Davis. Gastroenterology 118:S104-S114, 2000).

Additional References Disclosing Methods to Treat HCV Infections

A number of HCV treatments are reviewed by Bymock et al. in Antiviral Chemistry & Chemotherapy, 11:2; 79-95 (2000).

Several substrate-based NS3 protease inhibitors have been identified in the literature, in which the scissile amide bond of a cleaved substrate is replaced by an electrophile, which interacts with the catalytic serine. Attwood et al. (1998) Antiviral peptide derivatives, 98/22496; Attwood et al. (1999), Antiviral Chemistry and Chemotherapy 10.259-273; Attwood et al. (1999) Preparation and use of amino acid derivatives as anti-viral agents, German Patent Publication DE 19914474; Tung et al. (1998) Inhibitors of serine proteases, particularly hepatitis C virus NS3 protease, WO 98/17679. The reported inhibitors terminate in an electrophile such as a boronic acid or phosphonate. Llinas-Brunet et al. (1999) Hepatitis C inhibitor peptide analogues, WO 99/07734. Two classes of electrophile-based inhibitors have been described, alphaketoamides and hydrazinoureas.

The literature has also described a number of non-substrate-based inhibitors. For example, evaluation of the inhibitory effects of 2,4,6-trihydroxy-3-nitro-benzamide derivatives against HCV protease and other serine proteases has been reported. Sudo, K. et al., (1997) Biochemical and Biophysical Research Communications, 238:643-647; Sudo, K. et al. (1998) Antiviral Chemistry and Chemotherapy 9:186. Using a reverse-phase HPLC assay, the two most potent compounds identified were RD3-4082 and RD3-4078, the former substituted on the amide with a 14 carbon chain and the latter processing a para-phenoxyphenyl group.

Thiazolidine derivatives have been identified as micromolar inhibitors, using a reverse-phase HPLC assay with an NS3/4A fusion protein and NS5A/5B substrate. Sudo, K. et al. (1996) Antiviral Research 32:9-18. Compound RD-1-6250, possessing a fused cinnamoyl moiety substituted with a long alkyl chain, was the most potent against the isolated enzyme. Two other active examples were RD4 6205 and RD4 6193.

Other literature reports screening of a relatively small library using an ELISA assay and the identification of three compounds as potent inhibitors, a thiazolidine and two benzanilides. Kakiuchi N. et al. J. EBS Letters 421:217-220; Takeshita N. et al., Analytical Biochemistry 247:242-246, 1997. Several U.S. patents disclose protease inhibitors for the treatment of HCV. For example, U.S. Pat. No. 6,004,933 to Spruce et al. discloses a class of cysteine protease inhibitors for inhibiting HCV endopeptidase 2. U.S. Pat. No. 5,990,276 to Zhang et al. discloses synthetic inhibitors of hepatitis C virus NS3 protease. The inhibitor is a subsequence of a substrate of the NS3 protease or a substrate of the NS4A cofactor. The use of restriction enzymes to treat HCV is disclosed in U.S. Pat. No. 5,538,865 to Reyes et al.

Isolated from the fermentation culture broth of Streptomyces sp., Sch 68631, a phenan-threnequinone, possessed micromolar activity against HCV protease in a SDS-PAGE and autoradiography assay. Chu M. et al., Tetrahedron Letters 37:7229-7232, 1996. In another example by the same authors, Sch 351633, isolated from the fungus Penicillium griscofuluum, demonstrated micromolar activity in a scintillation proximity assay. Chu M. et al., Bioorganic and Medicinal Chemistry Letters 9:1949-1952. Nanomolar potency against the HCV NS3 protease enzyme has been achieved by the design of selective inhibitors based on the macromolecule eglin c. Eglin c, isolated from leech, is a potent inhibitor of several serine proteases such as S. griseus proteases A and B, α-chymotrypsin, chymase and subtilisin. Qasim M. A. et al., Biochemistry 36:1598-1607, 1997.

HCV helicase inhibitors have also been reported. U.S. Pat. No. 5,633,358 to Diana G. D. et al.; PCT Publication No. WO 97/36554 of Diana G. D. et al. There are a few reports of HCV polymerase inhibitors: some nucleotide analogues, gliotoxin and the natural product cerulenin. Ferrari R. et al., Journal of Virology 73:1649-1654, 1999; Lohmann V. et al., Virology 249:108-118, 1998.

Antisense phosphorothioate oligodeoxynucleotides complementary to sequence stretches in the 5′ non-coding region of the HCV, are reported as efficient inhibitors of HCV gene expression in in vitro translation and IIcpG2 IICV-luciferase cell culture systems. Alt M. et al., Hepatology 22:707-717, 1995. Recent work has demonstrated that nucleotides 326-348 comprising the 3′ end of the NCR and nucleotides 371-388 located in the core coding region of the HCV RNA are effective targets for antisense-mediated inhibition of viral translation. Alt M. et al., Archives of Virology 142:589-599, 1997. U.S. Pat. No. 6,001,990 to Wands et al. discloses oligonucleotides for inhibiting the replication of HCV. PCT Publication No. WO 99/29350 discloses compositions and methods of treatment for hepatitis C infection comprising the administration of antisense oligonucleotides that are complementary and hybridizable to HCV-RNA. U.S. Pat. No. 5,922,857 to Han et al. disclose nucleic acids corresponding to the sequence of the pestivirus homology box IV area for controlling the translation of HCV. Antisense oligonucleotides as therapeutic agents have been recently reviewed (Galderisi U. et al., Journal of Cellular Physiology 181:251-257, 1999).

Other compounds have been reported as inhibitors of IRES-dependent translation in HCV. Japanese Patent Publication JP-08268890 of Ikeda N et al.; Japanese Patent Publication JP-10101591 of Kai, Y. et al. Nuclease-resistant ribozymes have been targeted at the IRES and recently reported as inhibitors in an HCV-poliovirus chimera plaque assay. Maccjak D. J. et al., Hepatology 30 abstract 995, 1999. The use of ribozymes to treat HCV is also disclosed in U.S. Pat. No. 6,043,077 to Barber et al., and U.S. Pat. Nos. 5,869,253 and 5,610,054 to Draper et al.

Other patents disclose the use of immune system potentiating compounds for the treatment of HCV. For example, U.S. Pat. No. 6,001,799 to Chretien et al. discloses a method of treating hepatitis C in non-responders to interferon treatment by administering an immune system potentiating dose of thymosin or a thymosin fragment. U.S. Pat. Nos. 5,972,347 to Eder et al. and 5,969,109 to Bona et al. disclose antibody-based treatments for treating HCV.

U.S. Pat. No. 6,034,134 to Gold et al. discloses certain NMDA receptor agonists having immunodulatory, antimalarial, anti-Boma virus and anti-Hepatitis C activities. The disclosed NMDA receptor agonists belong to a family of 1-amino-alkylcyclohexanes. U.S. Pat. No. 6,030,960 to Morris-Natschke et al. discloses the use of certain alkyl lipids to inhibit the production of hepatitis-induced antigens, including those produced by the HCV virus. U.S. Pat. No. 5,922,757 to Chojkier et al. discloses the use of vitamin E and other antioxidants to treat hepatic disorders including HCV. U.S. Pat. No. 5,858,389 to Elsherbi et al. discloses the use of squalene for treating hepatitis C. U.S. Pat. No. 5,849,800 to Smith et al discloses the use of amantadine for treatment of Hepatitis C. U.S. Pat. No. 5,846,964 to Ozeki et al. discloses the use of bile acids for treating HCV. U.S. Pat. No. 5,491,135 to Blough et al. discloses the use of N-(phosphonoacetyl)-L-aspartic acid to treat flaviviruses such as HCV.

Other compounds proposed for treating HCV include plant extracts (U.S. Pat. No. 5,837,257 to Tsai et al., U.S. Pat. No. 5,725,859 to Omer et al., and U.S. Pat. No. 6,056,961), piperidenes (U.S. Pat. No. 5,830,905 to Diana et al.), benzenedicarboxamides (U.S. Pat. No. 5,633,388 to Diana et al.), polyadenylic acid derivatives (U.S. Pat. No. 5,496,546 to Wang et al.), 2′,3′-dideoxyinosine (U.S. Pat. No. 5,026,687 to Yarchoan et al.), benzimidazoles (U.S. Pat. No. 5,891,874 to Colacino et al.).

In light of the fact that the hepatitis C virus has reached epidemic levels worldwide, and has tragic effects on the infected patient, there remains a strong need to provide new effective pharmaceutical agents to treat hepatitis C that has low toxicity to the host.

Therefore, it is an object of the present invention to provide a compound, method and composition for the treatment of a host infected with hepatitis C virus.

SUMMARY OF THE INVENTION

Compounds, methods and compositions for the treatment of hepatitis C infection are described that include an effective hepatitis C treatment amount of a β-D- or β-L-nucleoside of the Formulas (I)-(XVIII), or a pharmaceutically acceptable salt or prodrug thereof.

In a first principal embodiment, a compound of Formula I, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: R¹, R² and R³ are independently H, phosphate (including mono-, di- or triphosphate and a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵ or SR⁴; X¹ and X² are independently selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵ or SR⁵; and R⁴ and R⁵ are independently hydrogen, acyl (including lower acyl), or alkyl (including but not limited to methyl, ethyl, propyl and cyclopropyl).

In a second principal embodiment, a compound of Formula II, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; and Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵ or SR⁴; X¹ and X² are independently selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵ or SR⁵; and R⁴ and R⁵ are independently hydrogen, acyl (including lower acyl), or alkyl (including but not limited to methyl, ethyl, propyl and cyclopropyl).

In a third principal embodiment, a compound of Formula III, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; and Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵ or SR⁴; X¹ and X² are independently selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵ or SR⁵; and R⁴ and R⁵ are independently hydrogen, acyl (including lower acyl), or alkyl (including but not limited to methyl, ethyl, propyl and cyclopropyl).

In a fourth principal embodiment, a compound of Formula IV, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: R¹, R² and R³ are independently H, phosphate (including mono-, di- or triphosphate and a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵ or SR⁴; X¹ is selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵ or SR⁵; and R⁴ and R⁵ are independently hydrogen, acyl (including lower acyl), or alkyl (including but not limited to methyl, ethyl, propyl and cyclopropyl).

In a fifth principal embodiment, a compound of Formula V, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; and Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵ or SR⁴; X¹ is selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵ or SR⁵; and R⁴ and R⁵ are independently hydrogen, acyl (including lower acyl), or alkyl (including but not limited to methyl, ethyl, propyl and cyclopropyl).

In a sixth principal embodiment, a compound of Formula VI, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; and Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵ or SR⁴; X¹ is selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵ or SR⁵; and R⁴ and R⁵ are independently hydrogen, acyl (including lower acyl), or alkyl (including but not limited to methyl, ethyl, propyl and cyclopropyl).

In a seventh principal embodiment, a compound selected from Formulas VII, VIII and IX, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, 2-Br-ethyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), CF₃, chloro, bromo, fluoro, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; and

X is O, S, SO₂ or CH₂.

In a eighth principal embodiment, a compound of Formulas X, XI and XII, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, fluoro, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R⁷ is hydrogen, OR³, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chlorine, bromine, iodine, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)_(2i) and

X is O, S, SO₂ or CH₂.

In a ninth principal embodiment a compound selected from Formulas XIII, XIV and XV, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, fluoro, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; and

X is O, S, SO₂ or CH₂.

In a tenth principal embodiment the invention provides a compound of Formula XVI, or a pharmaceutically acceptable salt or prodrug thereof:

wherein: Base is a purine or pyrimidine base as defined herein; R¹ and R² are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ or R² is independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, fluoro, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R⁷ and R⁹ are independently hydrogen, OR², hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chlorine, bromine, iodine, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R⁸ and R¹⁰ are independently H, alkyl (including lower alkyl), chlorine, bromine or iodine; alternatively, R⁷ and R⁹, R⁷ and R¹⁰, R⁸ and R⁹, or R⁸ and R¹⁰ can come together to form a pi bond; and

X is O, S, SO₂ or CH₂.

In a eleventh principal embodiment the invention provides a compound of Formula XVII, or a pharmaceutically acceptable salt or prodrug thereof:

wherein: Base is a purine or pyrimidine base as defined herein; R¹ and R² are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ or R² is independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, fluoro, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R⁷ and R⁹ are independently hydrogen, OR², hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chlorine, bromine, iodine, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R¹⁰ is H, alkyl (including lower alkyl), chlorine, bromine or iodine; alternatively, R⁷ and R⁹, or R⁷ and R¹⁰ can come together to form a pi bond; and

X is O, S, SO₂ or CH₂.

In an twelfth principal embodiment, the invention provides a compound of Formula XVIII, or a pharmaceutically acceptable salt or prodrug thereof:

wherein: Base is a purine or pyrimidine base as defined herein; R¹ and R² independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ or R² is independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, fluoro, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R⁷ and R⁹ are independently hydrogen, OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino or di(lower-alkyl)amino; R⁸ is H, alkyl (including lower alkyl), chlorine, bromine or iodine; alternatively, R⁷ and R⁹, or R⁸ and R⁹ can come together to form a pi bond;

X is O, S, SO₂ or CH₂.

The β-D- and β-L-nucleosides of this invention may inhibit HCV polymerase activity. Nucleosides can be screened for their ability to inhibit HCV polymerase activity in vitro according to screening methods set forth more particularly herein. One can readily determine the spectrum of activity by evaluating the compound in the assays described herein or with another confirmatory assay.

In one embodiment the efficacy of the anti-HCV compound is measured according to the concentration of compound necessary to reduce the plaque number of the virus in vitro, according to methods set forth more particularly herein, by 50% (i.e. the compound's EC₅₀). In preferred embodiments the compound exhibits an EC₅₀ of less than 25, 15, 10, 5, or 1 micromolar.

In another embodiment, the active compound can be administered in combination or alternation with another anti-HCV agent. In combination therapy, an effective dosage of two or more agents are administered together, whereas during alternation therapy an effective dosage of each agent is administered serially. The dosages will depend on absorption, inactivation, and excretion rates of the drug as well as other factors known to those of skill in the art. It is to be noted that dosage values will also vary with the severity of the condition to be alleviated. It is to be further understood that for any particular subject, specific dosage regimens and schedules should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions.

Nonlimiting examples of antiviral agents that can be used in combination with the compounds disclosed herein include:

(1) an interferon and/or ribavirin (Battaglia, A. M. et al., Ann. Pharmacother. 34:487-494, 2000); Berenguer, M. et al. Antivir. Ther. 3(Suppl. 3):125-136, 1998);

(2) Substrate-based NS3 protease inhibitors (Attwood et al., Antiviral peptide derivatives, PCT WO 98/22496, 1998; Attwood et al., Antiviral Chemistry and Chemotherapy 10.259-273, 1999; Attwood et al., Preparation and use of amino acid derivatives as anti-viral agents, German Patent Publication DE 19914474; Tung et al. Inhibitors of serine proteases, particularly hepatitis C virus NS3 protease, PCT WO 98/17679), including alphaketoamides and hydrazinoureas, and inhibitors that terminate in an electrophile such as a boronic acid or phosphonate. Llinas-Brunet et al, Hepatitis C inhibitor peptide analogues, PCT WO 99/07734.

(3) Non-substrate-based inhibitors such as 2,4,6-trihydroxy-3-nitro-benzamide derivatives (Sudo K. et al., Biochemical and Biophysical Research Communications, 238:643-647, 1997; Sudo K. et al. Antiviral Chemistry and Chemotherapy 9:186, 1998), including RD3-4082 and RD3-4078, the former substituted on the amide with a 14 carbon chain and the latter processing a para-phenoxyphenyl group;

(4) Thiazolidine derivatives which show relevant inhibition in a reverse-phase HPLC assay with an NS3/4A fusion protein and NS5A/5B substrate (Sudo K. et al., Antiviral Research 32:9-18, 1996), especially compound RD-1-6250, possessing a fused cinnamoyl moiety substituted with a long alkyl chain, RD4 6205 and RD4 6193;

(5) Thiazolidines and benzanilides identified in Kakiuchi N. et al. J. EBS Letters 421:217-220; Takeshita N. et al. Analytical Biochemistry 247:242-246, 1997;

(6) A phenan-threnequinone possessing activity against HCV protease in a SDS-PAGE and autoradiography assay isolated from the fermentation culture broth of Streptomyces sp., Sch 68631 (Chu M. et al., Tetrahedron Letters 37:7229-7232, 1996), and Sch 351633, isolated from the fungus Penicillium griscofuluum, which demonstrates activity in a scintillation proximity assay (Chu M. et al., Bioorganic and Medicinal Chemistry Letters 9:1949-1952);

(7) Selective NS3 inhibitors based on the macromolecule elgin c, isolated from leech (Qasim M. A. et al., Biochemistry 36:1598-1607, 1997);

(8) HCV helicase inhibitors (Diana G. D. et al., Compounds, compositions and methods for treatment of hepatitis C, U.S. Pat. No. 5,633,358; Diana G. D. et al., Piperidine derivatives, pharmaceutical compositions thereof and their use in the treatment of hepatitis C, PCT WO 97/36554);

(9) HCV polymerase inhibitors such as nucleotide analogues, gliotoxin (Ferrari R. et al. Journal of Virology 73:1649-1654, 1999), and the natural product cerulenin (Lohmann V. et al., Virology 249:108-118, 1998);

(10) Antisense phosphorothioate oligodeoxynucleotides (S-ODN) complementary to sequence stretches in the 5′ non-coding region (NCR) of the HCV (Alt M. et al., Hepatology 22:707-717, 1995), or nucleotides 326-348 comprising the 3′ end of the NCR and nucleotides 371-388 located in the core coding region of the IICV RNA (Alt M. et al., Archives of Virology 142:589-599, 1997; Galderisi U. et al., Journal of Cellular Physiology 181:251-257, 1999);

(11) Inhibitors of IRES-dependent translation (Ikeda N et al., Agent for the prevention and treatment of hepatitis C, Japanese Patent Publication JP-08268890; Kai Y. et al. Prevention and treatment of viral diseases, Japanese Patent Publication JP-10101591);

(12) Nuclease-resistant ribozymes (Maccjak D. J. et al., Hepatology 30 abstract 995, 1999); and

(13) Other miscellaneous compounds including 1-amino-alkylcyclohexanes (U.S. Pat. No. 6,034,134 to Gold et al.), alkyl lipids (U.S. Pat. No. 5,922,757 to Chojkier et al.), vitamin E and other antioxidants (U.S. Pat. No. 5,922,757 to Chojkier et al.), squalene, amantadine, bile acids (U.S. Pat. No. 5,846,964 to Ozeki et al.), N-(phosphonoacetyl)-L-aspartic acid, (U.S. Pat. No. 5,830,905 to Diana et al.), benzenedicarboxamides (U.S. Pat. No. 5,633,388 to Diana et al.), polyadenylic acid derivatives (U.S. Pat. No. 5,496,546 to Wang et al.), 2′,3′-dideoxyinosine (U.S. Pat. No. 5,026,687 to Yarchoan et al.), and benzimidazoles (U.S. Pat. No. 5,891,874 to Colacino et al.).

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 provides the structure of various non-limiting examples of nucleosides of the present invention, as well as other known nucleosides, FIAU and Ribavirin, which are used as comparative examples in the text.

FIG. 2 is a line graph of the pharmacokinetics (plasma concentrations) of β-D-2′-CH₃-riboG administered to six Cynomolgus Monkeys over time after administration.

FIGS. 3 a and 3 b are line graphs of the pharmacokinetics (plasma concentrations) of β-D-2′-CH₃-riboG administered to Cynomolgus Monkeys either intravenously (3a) or orally (3b) over time after administration.

DETAILED DESCRIPTION OF THE INVENTION

The invention as disclosed herein is a compound, method and composition for the treatment of hepatitis C in humans or other host animals, that includes administering an effective HCV treatment amount of a β-D- or β-L-nucleoside as described herein or a pharmaceutically acceptable salt or prodrug thereof, optionally in a pharmaceutically acceptable carrier. The compounds of this invention either possess antiviral (i.e., anti-HCV) activity, or are metabolized to a compound that exhibits such activity.

In summary, the present invention includes the following features:

(a) β-D- and β-L-nucleosides, as described herein, and pharmaceutically acceptable salts and prodrugs thereof;

(b) β-D- and β-L-nucleosides as described herein, and pharmaceutically acceptable salts and prodrugs thereof for use in the treatment or prophylaxis of an HCV infection, especially in individuals diagnosed as having an HCV infection or being at risk for becoming infected by HCV;

(c) use of these β-D- and β-L-nucleosides, and pharmaceutically acceptable salts and prodrugs thereof in the manufacture of a medicament for treatment of an HCV infection;

(d) pharmaceutical formulations comprising the β-D- or β-L-nucleosides or pharmaceutically acceptable salts or prodrugs thereof together with a pharmaceutically acceptable carrier or diluent;

(e) β-D- and β-L-nucleosides as described herein substantially in the absence of enantiomers of the described nucleoside, or substantially isolated from other chemical entities;

(f) processes for the preparation of β-D- and β-L-nucleosides, as described in more detail below; and

(g) processes for the preparation of β-D- and β-L-nucleosides substantially in the absence of enantiomers of the described nucleoside, or substantially isolated from other chemical entities.

I. Active Compound, and Physiologically Acceptable Salts and Prodrugs Thereof

In a first principal embodiment, a compound of Formula I, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: R¹, R² and R³ are independently H, phosphate (including mono-, di- or triphosphate and a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵ or SR⁴; X¹ and X² are independently selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵ or SR⁵; and R⁴ and R⁵ are independently hydrogen, acyl (including lower acyl), or alkyl (including but not limited to methyl, ethyl, propyl and cyclopropyl).

In a preferred subembodiment, a compound of Formula I, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

R¹, R² and R³ are independently H or phosphate (preferably H);

X¹ is H; X² is H or NH₂; and

Y is hydrogen, bromo, chloro, fluoro, iodo, NH₂ or OH.

In a second principal embodiment, a compound of Formula II, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; and Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵ or SR⁴; X¹ and X² are independently selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵ or SR⁵; and R⁴ and R⁵ are independently hydrogen, acyl (including lower acyl), or alkyl (including but not limited to methyl, ethyl, propyl and cyclopropyl).

In a preferred subembodiment, a compound of Formula II, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

R¹, R² and R³ are independently H or phosphate (preferably H);

X¹ is H; X² is H or NH₂; and

Y is hydrogen, bromo, chloro, fluoro, iodo, NH₂ or OH.

In a third principal embodiment, a compound of Formula III, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; and Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵ or SR⁴; X¹ and X² are independently selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵ or SR⁵; and R⁴ and R⁵ are independently hydrogen, acyl (including lower acyl), or alkyl (including but not limited to methyl, ethyl, propyl and cyclopropyl).

In a preferred subembodiment, a compound of Formula III, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

R¹, R² and R³ are independently H or phosphate (preferably H);

X¹ is H; X² is H or NH₂; and

Y is hydrogen, bromo, chloro, fluoro, iodo, NH₂ or OH.

In a fourth principal embodiment, a compound of Formula IV, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: R¹, R² and R³ are independently H, phosphate (including mono-, di- or triphosphate and a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵ or SR⁴; X¹ is selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵ or SR⁵; and R⁴ and R⁵ are independently hydrogen, acyl (including lower acyl), or alkyl (including but not limited to methyl, ethyl, propyl and cyclopropyl).

In a preferred subembodiment, a compound of Formula IV, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

R¹, R² and R³ are independently H or phosphate (preferably H);

X¹ is H or CH₃; and

Y is hydrogen, bromo, chloro, fluoro, iodo, NH₂ or OH.

In a fifth principal embodiment, a compound of Formula V, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; and Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵ or SR⁴; X¹ is selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵ or SR⁵; and R⁴ and R⁵ are independently hydrogen, acyl (including lower acyl), or alkyl (including but not limited to methyl, ethyl, propyl and cyclopropyl).

In a preferred subembodiment, a compound of Formula V, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

R¹, R² and R³ are independently H or phosphate (preferably H);

X¹ is H or CH₃; and

Y is hydrogen, bromo, chloro, fluoro, iodo, NH₂ or OH.

In a sixth principal embodiment, a compound of Formula VI, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; and Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵ or SR⁴; X¹ is selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵ or SR⁵; and R⁴ and R⁵ are independently hydrogen, acyl (including lower acyl), or alkyl (including but not limited to methyl, ethyl, propyl and cyclopropyl).

In a preferred subembodiment, a compound of Formula VI, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

R¹, R² and R³ are independently H or phosphate (preferably H);

X¹ is H or CH₃; and

Y is hydrogen, bromo, chloro, fluoro, iodo, NH₂ or OH.

In a seventh principal embodiment, a compound selected from Formulas VII, VIII and IX, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, 2-Br-ethyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), CF₃, chloro, bromo, fluoro, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; and

X is O, S, SO₂, or CH₂.

In a first preferred subembodiment, a compound of Formula VII, VIII or IX, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are independently hydrogen or phosphate; R⁶ is alkyl; and

X is O, S, SO₂ or CH₂.

In a second preferred subembodiment, a compound of Formula VII, VIII or IX, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are hydrogens; R⁶ is alkyl; and

X is O, S, SO₂ or CH₂.

In a third preferred subembodiment, a compound of Formula VII, VIII or IX, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are independently hydrogen or phosphate; R⁶ is alkyl; and

X is O.

In a eighth principal embodiment, a compound of Formula X, XI or XII, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, fluoro, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R⁷ is hydrogen, OR³, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chlorine, bromine, iodine, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(loweralkyl)₂, —N(acyl)₂; and

X is O, S, SO₂ or CH₂.

In a first preferred subembodiment, a compound of Formula X, XI or XII, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are independently hydrogen or phosphate; R⁶ is alkyl; and

X is O, S, SO₂ or CH₂.

In a second preferred subembodiment, a compound of Formula X, XI or XII, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are hydrogens; R⁶ is alkyl; and

X is O, S, SO₂ or CH₂.

In a third preferred subembodiment, a compound of Formula X, XI or XII, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are independently H or phosphate; R⁶ is alkyl; and

X is O.

In even more preferred subembodiments, a compound of Formula XI, or its pharmaceutically acceptable salt or prodrug, is provided:

wherein: Base is a purine or pyrimidine base as defined herein; optionally substituted with an amine or cyclopropyl (e.g., 2-amino, 2,6-diamino or cyclopropyl guanosine); and R¹ and R² are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ or R² is independently H or phosphate.

In a ninth principal embodiment a compound selected from Formula XIII, XIV or XV, or a pharmaceutically acceptable salt or prodrug thereof, is provided:

wherein: Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹, R² or R³ is independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, fluoro, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; and

X is O, S, SO₂ or CH₂.

In a first preferred subembodiment, a compound of Formula XIII, XIV or XV, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are independently hydrogen or phosphate; R⁶ is alkyl; and

X is O, S, SO₂ or CH₂.

In a second preferred subembodiment, a compound of Formula XIII, XIV or XV, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are hydrogens; R⁶ is alkyl; and

X is O, S, SO₂ or CH₂.

In a third preferred subembodiment, a compound of Formula XIII, XIV or XV, or a pharmaceutically acceptable salt or prodrug thereof, is provided wherein:

Base is a purine or pyrimidine base as defined herein; R¹, R² and R³ are independently hydrogen or phosphate; R⁶ is alkyl; and

X is O.

In a tenth principal embodiment the invention provides a compound of Formula XVI, or a pharmaceutically acceptable salt or prodrug thereof:

wherein: Base is a purine or pyrimidine base as defined herein; R¹ and R² are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ and R² are independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, fluoro, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R⁷ and R⁹ are independently hydrogen, OR², hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chlorine, bromine, iodine, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R⁸ and R¹⁰ are independently H, alkyl (including lower alkyl), chlorine, bromine or iodine; alternatively, R⁷ and R⁹, R⁷ and R¹⁰, R⁸ and R⁹, or R⁸ and R¹⁰ can come together to form a pi bond; and

X is O, S, SO₂ or CH₂.

In a first preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl; (4) R⁷ and R⁹ are independently OR², alkyl, alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (5) R⁸ and R¹⁰ are independently H, alkyl (including lower alkyl), chlorine, bromine, or iodine; and (6) X is O, S, SO₂ or CH₂.

In a second preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl, alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR²; (5) R⁸ and R¹⁰ are independently H, alkyl (including lower alkyl), chlorine, bromine, or iodine; and (6) X is O, S, SO₂ or CH₂.

In a third preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl, alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR², alkyl, alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (5) R⁸ and R¹⁰ are H; and (6) X is O, S, SO₂ or CH₂.

In a fourth preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl, alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR², alkyl, alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (5) R⁸ and R¹⁰ are independently H, alkyl (including lower alkyl), chlorine, bromine, or iodine; and (6) X is O.

In a fifth preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl; (4) R⁷ and R⁹ are independently OW; (5) R⁸ and R¹⁰ are independently H, alkyl (including lower alkyl), chlorine, bromine or iodine; and (6) X is O, S, SO₂ or CH₂.

In a sixth preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl; (4) R⁷ and R⁹ are independently OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (5) R⁸ and R¹⁰ are H; and (6) X is O, S, SO₂, or CH₂.

In a seventh preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl; (4) R⁷ and R⁹ are independently OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (5) R⁸ and R¹⁰ are independently H, alkyl (including lower alkyl), chlorine, bromine or iodine; and (6) X is O.

In a eighth preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR²; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O, S, SO₂ or CH₂.

In a ninth preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR²; (5) R⁸ and R¹⁰ are independently H, alkyl (including lower alkyl), chlorine, bromine or iodine; and (6) X is O.

In a tenth preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O.

In an eleventh preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR²; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O, S, SO₂ or CH₂.

In a twelfth preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate; (3) R⁶ is alkyl; (4) R⁷ and R⁹ are independently OR²; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O, S, SO₂, or CH₂.

In a thirteenth preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate; (3) R⁶ is alkyl; (4) R⁷ and R⁹ are independently OR²; (5) R⁸ and R¹⁰ are independently H, alkyl (including lower alkyl), chlorine, bromine, or iodine; and (6) X is O.

In a fourteenth preferred subembodiment, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate; (3) R⁶ is alkyl; (4) R⁷ and R⁹ are independently OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O.

In even more preferred subembodiments, a compound of Formula XVI, or its pharmaceutically acceptable salt or prodrug, is provided in which:

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O;

(1) Base is guanine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O;

(1) Base is cytosine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O;

(1) Base is thymine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O;

(1) Base is uracil; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is phosphate; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is ethyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is propyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is butyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ is hydrogen and R⁹ is hydroxyl; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is S;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is SO₂;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ and R¹⁰ are hydrogen; and (6) X is CH₂;

In a eleventh principal embodiment the invention provides a compound of Formula XVII, or a pharmaceutically acceptable salt or prodrug thereof:

wherein: Base is a purine or pyrimidine base as defined herein; R¹ is H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, fluoro, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R⁷ and R⁹ are independently hydrogen, OR², hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chlorine, bromine, iodine, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R¹⁰ is H alkyl (including lower alkyl), chlorine, bromine, or iodine; alternatively, R⁷ and R⁹, or R⁷ and R¹⁰ can come together to form a pi bond; and

X is O, S, SO₂ or CH₂.

In a first preferred subembodiment, a compound of Formula XVII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently hydrogen, OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino or di(loweralkyl)-amino; (5) R¹⁰ is H; and (6) X is O, S, SO₂, or CH₂.

In a second preferred subembodiment, a compound of Formula XVII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR²; (5) R¹⁰ is H, alkyl (including lower alkyl), chlorine, bromine, or iodine; and (6) X is O, S, SO₂ or CH₂.

In a third preferred subembodiment, a compound of Formula XVII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently hydrogen, OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino or di(loweralkyl)-amino; (5) R¹⁰ is H, alkyl (including lower alkyl), chlorine, bromine or iodine; and (6) X is O.

In a fourth preferred subembodiment, a compound of Formula XVII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR²; (5) R¹⁰ is H; and (6) X is O, S, SO₂ or CH₂.

In a fifth preferred subembodiment, a compound of Formula XVII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR²; (5) R¹⁰ is H, alkyl (including lower alkyl), chlorine, bromine or iodine; and (6) X is O.

In a sixth preferred subembodiment, a compound of Formula XVII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently hydrogen, OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (5) R¹⁰ is H; and (6) X is O.

In a seventh preferred subembodiment, a compound of Formula XVII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR²; (5) R¹⁰ is H; and (6) X is O.

In an eighth preferred subembodiment, a compound of Formula XVII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate; (3) R⁶ is alkyl; (4) R⁷ and R⁹ are independently hydrogen, OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino or di(loweralkyl)-amino; (5) R¹⁰ is H, alkyl (including lower alkyl), chlorine, bromine or iodine; and (6) X is O, S, SO₂, or CH₂.

In a ninth preferred subembodiment, a compound of Formula XVII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR²; (5) R¹⁰ is H; and (6) X is O, S, SO₂, or CH₂.

In a tenth preferred subembodiment, a compound of Formula XVII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate; (3) R⁶ is alkyl; (4) R⁷ and R⁹ are independently OR²; (5) R¹⁰ is H; and (6) X is O, S, SO₂, or CH₂.

In even more preferred subembodiments, a compound of Formula XVII, or its pharmaceutically acceptable salt or prodrug, is provided in which:

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R¹⁰ is hydrogen; and (6) X is O;

(1) Base is guanine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R¹⁰ is hydrogen; and (6) X is O;

(1) Base is cytosine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R¹⁰ is hydrogen; and (6) X is O;

(1) Base is thymine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R¹⁰ is hydrogen; and (6) X is O;

(1) Base is uracil; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R¹⁰ is hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is phosphate; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R¹⁰ is hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is ethyl; (4) R⁷ and R⁹ are hydroxyl; (5) R¹⁰ is hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is propyl; (4) R⁷ and R⁹ are hydroxyl; (5) R¹⁰ is hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is butyl; (4) R⁷ and R⁹ are hydroxyl; (5) R¹⁰ is hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R¹⁰ is hydrogen; and (6) X is S;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R¹⁰ is hydrogen; and (6) X is SO₂; or

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R¹⁰ is hydrogen; and (6) X is CH₂.

In an twelfth principal embodiment the invention provides a compound of Formula XVIII, or a pharmaceutically acceptable salt or prodrug thereof:

wherein: Base is a purine or pyrimidine base as defined herein; R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, fluoro, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R⁷ and R⁹ are independently hydrogen, OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, lower alkylamino, or di(loweralkyl)amino; R⁸ is H, alkyl (including lower alkyl), chlorine, bromine or iodine; alternatively, R⁷ and R⁹, or R⁸ and R⁹ can come together to form a pi bond;

X is O, S, SO₂ or CH₂.

In a first preferred subembodiment, a compound of Formula XVIII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl; (4) R⁷ and R⁹ are independently hydrogen, OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (5) R⁸ is H, alkyl (including lower alkyl), chlorine, bromine or iodine; and (6) X is O, S, SO₂ or CH₂.

In a second preferred subembodiment, a compound of Formula XVIII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino or di-(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR²; (5) R⁸ is H, alkyl (including lower alkyl), chlorine, bromine, or iodine; and (6) X is O, S, SO₂ or CH₂.

In a third preferred subembodiment, a compound of Formula XVIII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino, or di(lower-alkyl)amino; (4) R⁷ and R⁹ are independently hydrogen, OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (5) R⁸ is H; and (6) X is O, S, SO₂ or CH₂.

In a fourth preferred subembodiment, a compound of Formula XVIII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently hydrogen, OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (5) R⁸ is H, alkyl (including lower alkyl), chlorine, bromine, or iodine; and (6) X is O.

In a fifth preferred subembodiment, a compound of Formula XVIII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR²; (5) R⁸ is H; and (6) X is O, S, SO₂, or CH₂.

In a sixth preferred subembodiment, a compound of Formula XVIII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR²; (5) R⁸ is H, alkyl (including lower alkyl), chlorine, bromine, or iodine; and (6) X is O.

In a seventh preferred subembodiment, a compound of Formula XVIII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently hydrogen, OR², alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, O-alkenyl, chlorine, bromine, iodine, NO₂, amino, loweralkylamino, or di(loweralkyl)amino; (5) R⁸ is H; and (6) X is O.

In an eighth preferred subembodiment, a compound of Formula XVIII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate; (3) R⁶ is alkyl (including lower alkyl), alkenyl, alkynyl, Br-vinyl, hydroxy, O-alkyl, O-alkenyl, chloro, bromo, fluoro, iodo, NO₂, amino, loweralkylamino or di(loweralkyl)amino; (4) R⁷ and R⁹ are independently OR²; (5) R⁸ is H; and (6) X is O, S, SO₂ or CH₂.

In a ninth preferred subembodiment, a compound of Formula XVIII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate; (3) R⁶ is alkyl; (4) R⁷ and R⁹ are independently OR²; (5) R⁸ is H; and (6) X is O, S, SO₂, or CH₂.

In a tenth preferred subembodiment, a compound of Formula XVIII, or its pharmaceutically acceptable salt or prodrug, is provided in which: (1) Base is a purine or pyrimidine base as defined herein; (2) R¹ is independently H or phosphate; (3) R⁶ is alkyl; (4) R⁷ and R⁹ are independently OR²; (5) R⁸ is H; and (6) X is O.

In even more preferred subembodiments, a compound of Formula XVIII, or its pharmaceutically acceptable salt or prodrug, is provided in which:

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ is hydrogen; and (6) X is O;

(1) Base is guanine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ is hydrogen; and (6) X is O;

(1) Base is cytosine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ is hydrogen; and (6) X is O;

(1) Base is thymine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ is hydrogen; and (6) X is O;

(1) Base is uracil; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ is hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is phosphate; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ is hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is ethyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ is hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is propyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ is hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is butyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ is hydrogen; and (6) X is O;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ is hydrogen; and (6) X is S;

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ is hydrogen; and (6) X is SO₂; or

(1) Base is adenine; (2) R¹ is hydrogen; (3) R⁶ is methyl; (4) R⁷ and R⁹ are hydroxyl; (5) R⁸ is hydrogen; and (6) X is CH₂.

The β-D- and β-L-nucleosides of this invention may inhibit HCV polymerase activity. Nucleosides can be screened for their ability to inhibit HCV polymerase activity in vitro according to screening methods set forth more particularly herein. One can readily determine the spectrum of activity by evaluating the compound in the assays described herein or with another confirmatory assay.

In one embodiment the efficacy of the anti-HCV compound is measured according to the concentration of compound necessary to reduce the plaque number of the virus in vitro, according to methods set forth more particularly herein, by 50% (i.e. the compound's EC₅₀). In preferred embodiments the compound exhibits an EC₅₀ of less than 15 or 10 micromolar, when measured according to the polymerase assay described in Ferrari et al., Jnl. of Vir., 73:1649-1654, 1999; Ishii et al., Hepatology, 29:1227-1235, 1999; Lohmann et al., Jnl. of Bio. Chem., 274:10807-10815, 1999; or Yamashita et al, Jnl. of Bio. Chem., 273:15479-15486, 1998.

The active compound can be administered as any salt or prodrug that upon administration to the recipient is capable of providing directly or indirectly the parent compound, or that exhibits activity itself. Nonlimiting examples are the pharmaceutically acceptable salts (alternatively referred to as “physiologically acceptable salts”), and a compound that has been alkylated or acylated at the 5′-position or on the purine or pyrimidine base (a type of “pharmaceutically acceptable prodrug”). Further, the modifications can affect the biological activity of the compound, in some cases increasing the activity over the parent compound. This can easily be assessed by preparing the salt or prodrug and testing its antiviral activity according to the methods described herein, or other methods known to those skilled in the art.

II. Definitions

The term alkyl, as used herein, unless otherwise specified, refers to a saturated straight, branched, or cyclic, primary, secondary, or tertiary hydrocarbon of typically C₁ to C₁₀, and specifically includes methyl, ethyl, propyl, isopropyl, cyclopropyl, butyl, isobutyl, t-butyl, pentyl, cyclopentyl, isopentyl, neopentyl, hexyl, isohexyl, cyclohexyl, cyclohexylmethyl, 3-methylpentyl, 2,2-dimethylbutyl, and 2,3-dimethylbutyl. The term includes both substituted and unsubstituted alkyl groups. Moieties with which the alkyl group can be substituted are selected from the group consisting of hydroxyl, amino, alkylamino, arylamino, alkoxy, aryloxy, nitro, cyano, sulfonic acid, sulfate, phosphonic acid, phosphate, or phosphonate, either unprotected, or protected as necessary, as known to those skilled in the art, for example, as taught in Greene, et al., Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991, hereby incorporated by reference.

The term lower alkyl, as used herein, and unless otherwise specified, refers to a C₁ to C₄ saturated straight, branched, or if appropriate, a cyclic (for example, cyclopropyl) alkyl group, including both substituted and unsubstituted forms. Unless otherwise specifically stated in this application, when alkyl is a suitable moiety, lower alkyl is preferred. Similarly, when alkyl or lower alkyl is a suitable moiety, unsubstituted alkyl or lower alkyl is preferred.

The term alkylamino or arylamino refers to an amino group that has one or two alkyl or aryl substituents, respectively.

The term “protected” as used herein and unless otherwise defined refers to a group that is added to an oxygen, nitrogen, or phosphorus atom to prevent its further reaction or for other purposes. A wide variety of oxygen and nitrogen protecting groups are known to those skilled in the art of organic synthesis.

The term aryl, as used herein, and unless otherwise specified, refers to phenyl, biphenyl, or naphthyl, and preferably phenyl. The term includes both substituted and unsubstituted moieties. The aryl group can be substituted with one or more moieties selected from the group consisting of hydroxyl, amino, alkylamino, arylamino, alkoxy, aryloxy, nitro, cyano, sulfonic acid, sulfate, phosphonic acid, phosphate, or phosphonate, either unprotected, or protected as necessary, as known to those skilled in the art, for example, as taught in Greene, et al., Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991.

The term alkaryl or alkylaryl refers to an alkyl group with an aryl substituent. The term aralkyl or arylalkyl refers to an aryl group with an alkyl substituent.

The term halo, as used herein, includes chloro, bromo, iodo, and fluoro.

The term purine or pyrimidine base includes, but is not limited to, adenine, N⁶-alkylpurines, N⁶-acylpurines (wherein acyl is C(O)(alkyl, aryl, alkylaryl, or arylalkyl), N⁶-benzylpurine, N⁶-halopurine, N⁶-vinylpurine, N⁶-acetylenic purine, N⁶-acyl purine, N⁶-hydroxyalkyl purine, N⁶-thioalkyl purine, N²-alkylpurines, N²-alkyl-6-thiopurines, thymine, cytosine, 5-fluorocytosine, 5-methylcytosine, 6-azapyrimidine, including 6-azacytosine, 2- and/or 4-mercaptopyrmidine, uracil, 5-halouracil, including 5-fluorouracil, C⁵-alkylpyrimidines, C⁵-benzylpyrimidines, C⁵-halopyrimidines, C⁵-vinylpyrimidine, C⁵-acetylenic pyrimidine, C⁵-acyl pyrimidine, C⁵-hydroxyalkyl purine, C⁵-amidopyrimidine, C⁵-cyanopyrimidine, C⁵-nitropyrimidine, C⁵-aminopyrimidine, N²-alkylpurines, N²-alkyl-6-thiopurines, 5-azacytidinyl, 5-azauracilyl, triazolopyridinyl, imidazolopyridinyl, pyrrolopyrimidinyl, and pyrazolopyrimidinyl. Purine bases include, but are not limited to, guanine, adenine, hypoxanthine, 2,6-diaminopurine, and 6-chloropurine. Functional oxygen and nitrogen groups on the base can be protected as necessary or desired. Suitable protecting groups are well known to those skilled in the art, and include trimethylsilyl, dimethylhexylsilyl, t-butyldimethylsilyl, and t-butyldiphenylsilyl, trityl, alkyl groups, and acyl groups such as acetyl and propionyl, methanesulfonyl, and p-toluenesulfonyl.

The term acyl refers to a carboxylic acid ester in which the non-carbonyl moiety of the ester group is selected from straight, branched, or cyclic alkyl or lower alkyl, alkoxyalkyl including methoxymethyl, aralkyl including benzyl, aryloxyalkyl such as phenoxymethyl, aryl including phenyl optionally substituted with chloro, bromo, fluoro, iodo, C₁ to C₄ alkyl or C₁ to C₄ alkoxy, sulfonate esters such as alkyl or aralkyl sulphonyl including methanesulfonyl, the mono, di or triphosphate ester, trityl or monomethoxytrityl, substituted benzyl, trialkylsilyl (e.g. dimethyl-t-butylsilyl) or diphenylmethylsilyl. Aryl groups in the esters optimally comprise a phenyl group. The term “lower acyl” refers to an acyl group in which the non-carbonyl moiety is a lower alkyl.

As used herein, the term “substantially free of” or “substantially in the absence of refers to a nucleoside composition that includes at least 85 or 90% by weight, preferably 95% to 98% by weight, and even more preferably 99% to 100% by weight, of the designated enantiomer of that nucleoside. In a preferred embodiment, in the methods and compounds of this invention, the compounds are substantially free of enantiomers.

Similarly, the term “isolated” refers to a nucleoside composition that includes at least 85 or 90% by weight, preferably 95% to 98% by weight, and even more preferably 99% to 100% by weight, of the nucleoside, the remainder comprising other chemical species or enantiomers.

The term “independently” is used herein to indicate that the variable which is independently applied varies independently from application to application. Thus, in a compound such as R″XYR″, wherein R″ is “independently carbon or nitrogen,” both R″ can be carbon, both R″ can be nitrogen, or one R″ can be carbon and the other R″ nitrogen.

The term host, as used herein, refers to an unicellular or multicellular organism in which the virus can replicate, including cell lines and animals, and preferably a human. Alternatively, the host can be carrying a part of the hepatitis C viral genome, whose replication or function can be altered by the compounds of the present invention. The term host specifically refers to infected cells, cells transfected with all or part of the HCV genome and animals, in particular, primates (including chimpanzees) and humans. In most animal applications of the present invention, the host is a human patient. Veterinary applications, in certain indications, however, are clearly anticipated by the present invention (such as chimpanzees).

The term “pharmaceutically acceptable salt or prodrug” is used throughout the specification to describe any pharmaceutically acceptable form (such as an ester, phosphate ester, salt of an ester or a related group) of a nucleoside compound which, upon administration to a patient, provides the nucleoside compound. Pharmaceutically acceptable salts include those derived from pharmaceutically acceptable inorganic or organic bases and acids. Suitable salts include those derived from alkali metals such as potassium and sodium, alkaline earth metals such as calcium and magnesium, among numerous other acids well known in the pharmaceutical art. Pharmaceutically acceptable prodrugs refer to a compound that is metabolized, for example hydrolyzed or oxidized, in the host to form the compound of the present invention. Typical examples of prodrugs include compounds that have biologically labile protecting groups on a functional moiety of the active compound. Prodrugs include compounds that can be oxidized, reduced, aminated, deaminated, hydroxylated, dehydroxylated, hydrolyzed, dehydrolyzed, alkylated, dealkylated, acylated, deacylated, phosphorylated, dephosphorylated to produce the active compound. The compounds of this invention possess antiviral activity against HCV, or are metabolized to a compound that exhibits such activity.

III. Nucleotide Salt or Prodrug Formulations

In cases where compounds are sufficiently basic or acidic to form stable nontoxic acid or base salts, administration of the compound as a pharmaceutically acceptable salt may be appropriate. Examples of pharmaceutically acceptable salts are organic acid addition salts formed with acids, which form a physiological acceptable anion, for example, tosylate, methanesulfonate, acetate, citrate, malonate, tartarate, succinate, benzoate, ascorbate, a-ketoglutarate, and a-glycerophosphate. Suitable inorganic salts may also be formed, including, sulfate, nitrate, bicarbonate, and carbonate salts.

Pharmaceutically acceptable salts may be obtained using standard procedures well known in the art, for example by reacting a sufficiently basic compound such as an amine with a suitable acid affording a physiologically acceptable anion. Alkali metal (for example, sodium, potassium or lithium) or alkaline earth metal (for example calcium) salts of carboxylic acids can also be made.

Any of the nucleosides described herein can be administered as a nucleotide prodrug to increase the activity, bioavailability, stability or otherwise alter the properties of the nucleoside. A number of nucleotide prodrug ligands are known. In general, alkylation, acylation or other lipophilic modification of the mono, di or triphosphate of the nucleoside will increase the stability of the nucleotide. Examples of substituent groups that can replace one or more hydrogens on the phosphate moiety are alkyl, aryl, steroids, carbohydrates, including sugars, 1,2-diacylglycerol and alcohols. Many are described in R. Jones and N. Bischofberger, Antiviral Research, 27 (1995) 1-17. Any of these can be used in combination with the disclosed nucleosides to achieve a desired effect.

The active nucleoside can also be provided as a 5′-phosphoether lipid or a 5′-ether lipid, as disclosed in the following references, which are incorporated by reference herein: Kucera, L. S., N. Iyer, E. Leake, A. Raben, Modest E. K., D. L. W., and C. Piantadosi. 1990. “Novel membrane-interactive ether lipid analogs that inhibit infectious HIV-1 production and induce defective virus formation.” AIDS Res. Hum. Retro Viruses. 6:491-501; Piantadosi, C., J. Marasco C. J., S. L. Morris-Natschke, K. L. Meyer, F. Gumus, J. R. Surles, K. S. Ishaq, L. S. Kucera, N. Iyer, C. A.

Wallen, S. Piantadosi, and E. J. Modest. 1991. “Synthesis and evaluation of novel ether lipid nucleoside conjugates for anti-HIV activity.” J. Med. Chem. 34:1408.1414; Hosteller, K. Y., D. D. Richman, D. A. Carson, L. M. Stuhmiller, G. M. T. van Wijk, and H. van den Bosch. 1992. “Greatly enhanced inhibition of human immunodeficiency virus type 1 replication in CEM and HT4-6C cells by 3′-deoxythymidine diphosphate dimyristoylglycerol, a lipid prodrug of 3,-deoxythymidine.” Antimicrob. Agents Chemother. 36:2025.2029; Hosetler, K. Y., L. M. Stuhmiller, H. B. Lenting, H. van den Bosch, and D. D. Richman, 1990. “Synthesis and antiretroviral activity of phospholipid analogs of azidothymidine and other antiviral nucleosides.” J. Biol. Chem. 265:61127.

Nonlimiting examples of U.S. patents that disclose suitable lipophilic substituents that can be covalently incorporated into the nucleoside, preferably at the 5′-OH position of the nucleoside or lipophilic preparations, include U.S. Pat. Nos. 5,149,794 (Sep. 22, 1992, Yatvin et al.); 5,194,654 (Mar. 16, 1993, Hostetler et al., 5,223,263 (Jun. 29, 1993, Hostetler et al.); 5,256,641 (Oct. 26, 1993, Yatvin et al.); 5,411,947 (May 2, 1995, Hostetler et al.); 5,463,092 (Oct. 31, 1995, Hostetler et al.); 5,543,389 (Aug. 6, 1996, Yatvin et al.); 5,543,390 (Aug. 6, 1996, Yatvin et al.); 5,543,391 (Aug. 6, 1996, Yatvin et al.); and 5,554,728 (Sep. 10, 1996; Basava et al.), all of which are incorporated herein by reference. Foreign patent applications that disclose lipophilic substituents that can be attached to the nucleosides of the present invention, or lipophilic preparations, include WO 89/02733, WO 90/00555, WO 91/16920, WO 91/18914, WO 93/00910, WO 94/26273, WO 96/15132, EP 0 350 287, EP 93917054.4, and WO 91/19721.

IV. Combination and Alternation Therapy

It has been recognized that drug-resistant variants of HCV can emerge after prolonged treatment with an antiviral agent. Drug resistance most typically occurs by mutation of a gene that encodes for an enzyme used in viral replication. The efficacy of a drug against HCV infection can be prolonged, augmented, or restored by administering the compound in combination or alternation with a second, and perhaps third, antiviral compound that induces a different mutation from that caused by the principle drug. Alternatively, the pharmacokinetics, biodistribution or other parameter of the drug can be altered by such combination or alternation therapy. In general, combination therapy is typically preferred over alternation therapy because it induces multiple simultaneous stresses on the virus.

Nonlimiting examples of antiviral agents that can be used in combination with the compounds disclosed herein include:

(1) an interferon and/or ribavirin (Battaglia, A. M. et al., Ann. Pharmacother. 34:487-494, 2000); Berenguer, M. et al. Antivir. Ther. 3(Suppl. 3):125-136, 1998);

(2) Substrate-based NS3 protease inhibitors (Attwood et al., Antiviral peptide derivatives, PCT WO 98/22496, 1998; Attwood et al., Antiviral Chemistry and Chemotherapy 10.259-273, 1999; Attwood et al., Preparation and use of amino acid derivatives as anti-viral agents, German Patent Publication DE 19914474; Tung et al. Inhibitors of serine proteases, particularly hepatitis C virus NS3 protease, PCT WO 98/17679), including alphaketoamides and hydrazinoureas, and inhibitors that terminate in an electrophile such as a boronic acid or phosphonate. Llinas-Brunet et al, Hepatitis C inhibitor peptide analogues, PCT WO 99/07734.

(3) Non-substrate-based inhibitors such as 2,4,6-trihydroxy-3-nitro-benzamide derivatives (Sudo K. et al., Biochemical and Biophysical Research Communications, 238:643-647, 1997; Sudo K. et al. Antiviral Chemistry and Chemotherapy 9:186, 1998), including RD3-4082 and RD3-4078, the former substituted on the amide with a 14 carbon chain and the latter processing a para-phenoxyphenyl group;

(4) Thiazolidine derivatives which show relevant inhibition in a reverse-phase HPLC assay with an NS3/4A fusion protein and NS5A/5B substrate (Sudo K. et al., Antiviral Research 32:9-18, 1996), especially compound RD-1-6250, possessing a fused cinnamoyl moiety substituted with a long alkyl chain, RD4 6205 and RD4 6193;

(5) Thiazolidines and benzanilides identified in Kakiuchi N. et al. J. EBS Letters 421:217-220; Takeshita N. et al. Analytical Biochemistry 247:242-246, 1997;

(6) A phenan-threnequinone possessing activity against HCV protease in a SDS-PAGE and autoradiography assay isolated from the fermentation culture broth of Streptomyces sp., Sch 68631 (Chu M. et al., Tetrahedron Letters 37:7229-7232, 1996), and Sch 351633, isolated from the fungus Penicillium griscofuluum, which demonstrates activity in a scintillation proximity assay (Chu M. et al., Bioorganic and Medicinal Chemistry Letters 9:1949-1952);

(7) Selective NS3 inhibitors based on the macromolecule elgin c, isolated from leech (Qasim M. A. et al., Biochemistry 36:1598-1607, 1997);

(8) HCV helicase inhibitors (Diana G. D. et al., Compounds, compositions and methods for treatment of hepatitis C, U.S. Pat. No. 5,633,358; Diana G. D. et al., Piperidine derivatives, pharmaceutical compositions thereof and their use in the treatment of hepatitis C, PCT WO 97/36554);

(9) HCV polymerase inhibitors such as nucleotide analogues, gliotoxin (Ferrari R. et al. Journal of Virology 73:1649-1654, 1999), and the natural product cerulenin (Lohmann V. et al., Virology 249:108-118, 1998);

(10) Antisense phosphorothioate oligodeoxynucleotides (S-ODN) complementary to sequence stretches in the 5′ non-coding region (NCR) of the HCV (Alt M. et al., Hepatology 22:707-717, 1995), or nucleotides 326-348 comprising the 3′ end of the NCR and nucleotides 371-388 located in the core coding region of the IICV RNA (Alt M. et al., Archives of Virology 142:589-599, 1997; Galderisi U. et al., Journal of Cellular Physiology 181:251-257, 1999);

(11) Inhibitors of IRES-dependent translation (Ikeda N et al., Agent for the prevention and treatment of hepatitis C, Japanese Patent Publication JP-08268890; Kai Y. et al. Prevention and treatment of viral diseases, Japanese Patent Publication JP-10101591);

(12) Nuclease-resistant ribozymes. (Maccjak D. J. et al., Hepatology 30 abstract 995, 1999); and

(13) Other miscellaneous compounds including 1-amino-alkylcyclohexanes (U.S. Pat. No. 6,034,134 to Gold et al.), alkyl lipids (U.S. Pat. No. 5,922,757 to Chojkier et al.), vitamin E and other antioxidants (U.S. Pat. No. 5,922,757 to Chojkier et al.), squalene, amantadine, bile acids (U.S. Pat. No. 5,846,964 to Ozeki et al.), N-(phosphonoacetyl)-L-aspartic acid, (U.S. Pat. No. 5,830,905 to Diana et al.), benzenedicarboxamides (U.S. Pat. No. 5,633,388 to Diana et al.), polyadenylic acid derivatives (U.S. Pat. No. 5,496,546 to Wang et al.), 2′,3′-dideoxyinosine (U.S. Pat. No. 5,026,687 to Yarchoan et al.), and benzimidazoles (U.S. Pat. No. 5,891,874 to Colacino et al.).

V. Pharmaceutical Compositions

Hosts, including humans, infected with HCV, or a gene fragment thereof, can be treated by administering to the patient an effective amount of the active compound or a pharmaceutically acceptable prodrug or salt thereof in the presence of a pharmaceutically acceptable carrier or diluent. The active materials can be administered by any appropriate route, for example, orally, parenterally, intravenously, intradermally, subcutaneously, or topically, in liquid or solid form.

A preferred dose of the compound for HCV will be in the range from about 1 to 50 mg/kg, preferably 1 to 20 mg/kg, of body weight per day, more generally 0.1 to about 100 mg per kilogram body weight of the recipient per day. The effective dosage range of the pharmaceutically acceptable salts and prodrugs can be calculated based on the weight of the parent nucleoside to be delivered. If the salt or prodrug exhibits activity in itself, the effective dosage can be estimated as above using the weight of the salt or prodrug, or by other means known to those skilled in the art.

The compound is conveniently administered in unit any suitable dosage form, including but not limited to one containing 7 to 3000 mg, preferably 70 to 1400 mg of active ingredient per unit dosage form. A oral dosage of 50-1000 mg is usually convenient.

Ideally the active ingredient should be administered to achieve peak plasma concentrations of the active compound of from about 0.2 to 70 μM, preferably about 1.0 to 10 μM. This may be achieved, for example, by the intravenous injection of a 0.1 to 5% solution of the active ingredient, optionally in saline, or administered as a bolus of the active ingredient.

The concentration of active compound in the drug composition will depend on absorption, inactivation and excretion rates of the drug as well as other factors known to those of skill in the art. It is to be noted that dosage values will also vary with the severity of the condition to be alleviated. It is to be further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions, and that the concentration ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the claimed composition. The active ingredient may be administered at once, or may be divided into a number of smaller doses to be administered at varying intervals of time.

A preferred mode of administration of the active compound is oral. Oral compositions will generally include an inert diluent or an edible carrier. They may be enclosed in gelatin capsules or compressed into tablets. For the purpose of oral therapeutic administration, the active compound can be incorporated with excipients and used in the form of tablets, troches, or capsules. Pharmaceutically compatible binding agents, and/or adjuvant materials can be included as part of the composition.

The tablets, pills, capsules, troches and the like can contain any of the following ingredients, or compounds of a similar nature: a binder such as microcrystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch; a lubricant such as magnesium stearate or Sterotes; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring. When the dosage unit form is a capsule, it can contain, in addition to material of the above type, a liquid carrier such as a fatty oil. In addition, dosage unit forms can contain various other materials which modify the physical form of the dosage unit, for example, coatings of sugar, shellac, or other enteric agents.

The compound can be administered as a component of an elixir, suspension, syrup, wafer, chewing gum or the like. A syrup may contain, in addition to the active compounds, sucrose as a sweetening agent and certain preservatives, dyes and colorings and flavors.

The compound or a pharmaceutically acceptable prodrug or salts thereof can also be mixed with other active materials that do not impair the desired action, or with materials that supplement the desired action, such as antibiotics, antifungals, anti-inflammatories, or other antivirals, including other nucleoside compounds. Solutions or suspensions used for parenteral, intradermal, subcutaneous, or topical application can include the following components: a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents; antibacterial agents such as benzyl alcohol or methyl parabens; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as ethylenediaminetetraacetic acid; buffers such as acetates, citrates or phosphates and agents for the adjustment of tonicity such as sodium chloride or dextrose. The parental preparation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic.

If administered intravenously, preferred carriers are physiological saline or phosphate buffered saline (PBS).

In a preferred embodiment, the active compounds are prepared with carriers that will protect the compound against rapid elimination from the body, such as a controlled release formulation, including implants and microencapsulated delivery systems. Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters and polylactic acid. Methods for preparation of such formulations will be apparent to those skilled in the art. The materials can also be obtained commercially from Alza Corporation.

Liposomal suspensions (including liposomes targeted to infected cells with monoclonal antibodies to viral antigens) are also preferred as pharmaceutically acceptable carriers. These may be prepared according to methods known to those skilled in the art, for example, as described in U.S. Pat. No. 4,522,811 (which is incorporated herein by reference in its entirety). For example, liposome formulations may be prepared by dissolving appropriate lipid(s) (such as stearoyl phosphatidyl ethanolamine, stearoyl phosphatidyl choline, arachadoyl phosphatidyl choline, and cholesterol) in an inorganic solvent that is then evaporated, leaving behind a thin film of dried lipid on the surface of the container. An aqueous solution of the active compound or its monophosphate, diphosphate, and/or triphosphate derivatives is then introduced into the container. The container is then swirled by hand to free lipid material from the sides of the container and to disperse lipid aggregates, thereby forming the liposomal suspension.

VI. Processes for the Preparation of Active Compounds

The nucleosides of the present invention can be synthesized by any means known in the art. In particular, the synthesis of the present nucleosides can be achieved by either alkylating the appropriately modified sugar, followed by glycosylation or glycosylation followed by alkylation of the nucleoside. The following non-limiting embodiments illustrate some general methodology to obtain the nucleosides of the present invention.

A. General Synthesis of 1′-C-Branched Nucleosides

1′-C-Branched ribonucleosides of the following structure:

wherein BASE is a purine or pyrimidine base as defined herein; R⁷ and R⁹ are independently hydrogen, OR², hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chlorine, bromine, iodine, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R⁸ and R¹⁰ are independently H, alkyl (including lower alkyl), chlorine, bromine or iodine; alternatively, R⁷ and R⁹, R⁷ and R¹⁰, R⁸ and R⁹, or R⁸ and R¹⁰ can come together to form a pi bond; R¹ and R² are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ or R² is independently H or phosphate; R⁶ is an alkyl, chloro-, bromo-, fluoro-, or iodo-alkyl (i.e. CF₃), alkenyl, or alkynyl (i.e. allyl); and

X is O, S, SO₂ or CH₂

can be prepared by one of the following general methods. 1) Modification from the Lactone

The key starting material for this process is an appropriately substituted lactone. The lactone can be purchased or can be prepared by any known means including standard epimerization, substitution and cyclization techniques. The lactone can be optionally protected with a suitable protecting group, preferably with an acyl or silyl group, by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991. The protected lactone can then be coupled with a suitable coupling agent, such as an organometallic carbon nucleophile, such as a Grignard reagent, an organolithium, lithium dialkylcopper or R⁶—SiMe₃ in TBAF with the appropriate non-protic solvent at a suitable temperature, to give the 1′-alkylated sugar.

The optionally activated sugar can then be coupled to the BASE by methods well known to those skilled in the art, as taught by Townsend Chemistry of Nucleosides and Nucleotides, Plenum Press, 1994. For example, an acylated sugar can be coupled to a silylated base with a lewis acid, such as tin tetrachloride, titanium tetrachloride or trimethylsilyltriflate in the appropriate solvent at a suitable temperature.

Subsequently, the nucleoside can be deprotected by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991.

In a particular embodiment, the 1′-C-branched ribonucleoside is desired. The synthesis of a ribonucleoside is shown in Scheme 1. Alternatively, deoxyribo-nucleoside is desired. To obtain these nucleosides, the formed ribonucleoside can optionally be protected by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991, and then the 2′-OH can be reduced with a suitable reducing agent. Optionally, the 2′-hydroxyl can be activated to facilitate reduction; i.e. via the Barton reduction.

2. Alternative Method for the Preparation of 1′-C-Branched Nucleosides

The key starting material for this process is an appropriately substituted hexose. The hexose can be purchased or can be prepared by any known means including standard epimerization, such as alkaline treatment, substitution and coupling techniques. The hexose can be selectively protected to give the appropriate hexa-furanose, as taught by Townsend Chemistry of Nucleosides and Nucleotides, Plenum Press, 1994.

The 1′-hydroxyl can be optionally activated to a suitable leaving group such as an acyl group or a chloro, bromo, fluoro, iodo via acylation or halogenation, respectively. The optionally activated sugar can then be coupled to the BASE by methods well known to those skilled in the art, as taught by Townsend Chemistry of Nucleosides and Nucleotides, Plenum Press, 1994. For example, an acylated sugar can be coupled to a silylated base with a lewis acid, such as tin tetrachloride, titanium tetrachloride or trimethylsilyltriflate in the appropriate solvent at a suitable temperature. Alternatively, a halo-sugar can be coupled to a silylated base with the presence of trimethylsilyltriflate.

The 1′-CH₂—OH, if protected, can be selectively deprotected by methods well known in the art. The resultant primary hydroxyl can be functionalized to yield various C-branched nucleosides. For example, the primary hydroxyl can be reduced to give the methyl, using a suitable reducing agent. Alternatively, the hydroxyl can be activated prior to reduction to facilitate the reaction; i.e. via the Barton reduction. In an alternate embodiment, the primary hydroxyl can be oxidized to the aldehyde, then coupled with a carbon nucleophile, such as a Grignard reagent, an organolithium, lithium dialkylcopper or R⁶—SiMe₃ in TBAF with the appropriate non-protic solvent at a suitable temperature.

In a particular embodiment, the 1′-C-branched ribonucleoside is desired. The synthesis of a ribonucleoside is shown in Scheme 2. Alternatively, deoxyribo-nucleoside is desired. To obtain these nucleosides, the formed ribonucleoside can optionally be protected by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991, and then the 2′-OH can be reduced with a suitable reducing agent. Optionally, the 2′-hydroxyl can be activated to facilitate reduction; i.e. via the Barton reduction.

In addition, the L-enantiomers corresponding to the compounds of the invention can be prepared following the same general methods (1 or 2), beginning with the corresponding L-sugar or nucleoside L-enantiomer as starting material.

B. General Synthesis of 2′-C-Branched Nucleosides

2′-C-Branched ribonucleosides of the following structure:

wherein BASE is a purine or pyrimidine base as defined herein; R⁷ and R⁹ are independently hydrogen, OR², hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chlorine, bromine, iodine, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R¹⁰ is H, H alkyl (including lower alkyl), chlorine, bromine or iodine; alternatively, R⁷ and R⁹, or R⁷ and R₁₀ can come together to form a pi bond; R¹ and R² are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ or R² is independently H or phosphate; R⁶ is an alkyl, chloro-, bromo-, fluoro-, iodo-alkyl (i.e. CF₃), alkenyl, or alkynyl (i.e. allyl); and

X is O, S, SO₂ or CH₂

can be prepared by one of the following general methods. 1. Glycosylation of the Nucleobase with an Appropriately Modified Sugar

The key starting material for this process is an appropriately substituted sugar with a 2′-OH and 2′-H, with the appropriate leaving group (LG), for example an acyl group or a chloro, bromo, fluoro or iodo. The sugar can be purchased or can be prepared by any known means including standard epimerization, substitution, oxidation and reduction techniques. The substituted sugar can then be oxidized with the appropriate oxidizing agent in a compatible solvent at a suitable temperature to yield the 2′-modified sugar. Possible oxidizing agents are Jones reagent (a mixture of chromic acid and sulfuric acid), Collins's reagent (dipyridine Cr(VI) oxide, Corey's reagent (pyridinium chlorochromate), pyridinium dichromate, acid dichromate, potassium permanganate, MnO₂, ruthenium tetroxide, phase transfer catalysts such as chromic acid or permanganate supported on a polymer, Cl₂-pyridine, H₂O₂-ammonium molybdate, NaBrO₂—CAN, NaOCl in HOAc, copper chromite, copper oxide, Raney nickel, palladium acetate, Meerwin-Pondorf-Verley reagent (aluminum t-butoxide with another ketone) and N-bromosuccinimide

Then coupling of an organometallic carbon nucleophile, such as a Grignard reagent, an organolithium, lithium dialkylcopper or R⁶—SiMe₃ in TBAF with the ketone with the appropriate non-protic solvent at a suitable temperature, yields the 2′-alkylated sugar. The alkylated sugar can be optionally protected with a suitable protecting group, preferably with an acyl or silyl group, by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991.

The optionally protected sugar can then be coupled to the BASE by methods well known to those skilled in the art, as taught by Townsend Chemistry of Nucleosides and Nucleotides, Plenum Press, 1994. For example, an acylated sugar can be coupled to a silylated base with a lewis acid, such as tin tetrachloride, titanium tetrachloride or trimethylsilyltriflate in the appropriate solvent at a suitable temperature. Alternatively, a halo-sugar can be coupled to a silylated base with the presence of trimethylsilyltriflate.

Subsequently, the nucleoside can be deprotected by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991.

In a particular embodiment, the 2′-C-branched ribonucleoside is desired. The synthesis of a ribonucleoside is shown in Scheme 3. Alternatively, deoxyribo-nucleoside is desired. To obtain these nucleosides, the formed ribonucleoside can optionally be protected by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991, and then the 2′-OH can be reduced with a suitable reducing agent. Optionally, the 2′-hydroxyl can be activated to facilitate reduction; i.e. via the Barton reduction.

2. Modification of a Pre-Formed Nucleoside

The key starting material for this process is an appropriately substituted nucleoside with a 2′-OH and 2′-H. The nucleoside can be purchased or can be prepared by any known means including standard coupling techniques. The nucleoside can be optionally protected with suitable protecting groups, preferably with acyl or silyl groups, by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991.

The appropriately protected nucleoside can then be oxidized with the appropriate oxidizing agent in a compatible solvent at a suitable temperature to yield the 2′-modified sugar. Possible oxidizing agents are Jones reagent (a mixture of chromic acid and sulfuric acid), Collins's reagent (dipyridine Cr(VI) oxide, Corey's reagent (pyridinium chlorochromate), pyridinium dichromate, acid dichromate, potassium permanganate, MnO₂, ruthenium tetroxide, phase transfer catalysts such as chromic acid or permanganate supported on a polymer, Cl₂-pyridine, H₂O₂-ammonium molybdate, NaBrO₂—CAN, NaOCl in HOAc, copper chromite, copper oxide, Raney nickel, palladium acetate, Meerwin-Pondorf-Verley reagent (aluminum t-butoxide with another ketone) and N-bromosuccinimide.

Subsequently, the nucleoside can be deprotected by methods well known to those skilled in the art, as taught by GreeneGreene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991.

In a particular embodiment, the 2′-C-branched ribonucleoside is desired. The synthesis of a ribonucleoside is shown in Scheme 4. Alternatively, deoxyribo-nucleoside is desired. To obtain these nucleosides, the formed ribonucleoside can optionally be protected by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991, and then the 2′-OH can be reduced with a suitable reducing agent. Optionally, the 2′-hydroxyl can be activated to facilitate reduction; i.e. via the Barton reduction.

In another embodiment of the invention, the L-enantiomers are desired. Therefore, the L-enantiomers can be corresponding to the compounds of the invention can be prepared following the same foregoing general methods, beginning with the corresponding L-sugar or nucleoside L-enantiomer as starting material.

C. General Synthesis of 3′-C-Branched Nucleosides

3′-C-Branched ribonucleosides of the following structure:

wherein BASE is a purine or pyrimidine base as defined herein; R⁷ and R⁹ are independently hydrogen, OR², hydroxy, alkyl (including lower alkyl), azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chlorine, bromine, iodine, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, —N(acyl)₂; R⁸ is H, alkyl (including lower alkyl), chlorine, bromine or iodine; alternatively, R⁷ and R⁹, or R⁸ and R⁹ can come together to form a pi bond; R¹ and R² are independently H; phosphate (including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug); acyl (including lower acyl); alkyl (including lower alkyl); sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl and benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given herein; a lipid, including a phospholipid; an amino acid; a carbohydrate; a peptide; a cholesterol; or other pharmaceutically acceptable leaving group which when administered in vivo is capable of providing a compound wherein R¹ or R² is independently H or phosphate; R⁶ is an alkyl, chloro-, fluoro-, bromo-, iodo-alkyl (i.e. CF₃), alkenyl, or alkynyl (i.e. allyl); and

X is O, S, SO₂ or CH₂

can be prepared by one of the following general methods. 1. Glycosylation of the Nucleobase with an Appropriately Modified Sugar

The key starting material for this process is an appropriately substituted sugar with a 3′-OH and 3′-H, with the appropriate leaving group (LG), for example an acyl group or a chloro, bromo, fluoro, iodo. The sugar can be purchased or can be prepared by any known means including standard epimerization, substitution, oxidation and reduction techniques. The substituted sugar can then be oxidized with the appropriate oxidizing agent in a compatible solvent at a suitable temperature to yield the 3′-modified sugar. Possible oxidizing agents are Jones reagent (a mixture of chromic acid and sulfuric acid), Collins's reagent (dipyridine Cr(VI) oxide, Corey's reagent (pyridinium chlorochromate), pyridinium dichromate, acid dichromate, potassium permanganate, MnO₂, ruthenium tetroxide, phase transfer catalysts such as chromic acid or permanganate supported on a polymer, Cl₂-pyridine, H₂O₂-ammonium molybdate, NaBrO₂—CAN, NaOCl in HOAc, copper chromite, copper oxide, Raney nickel, palladium acetate, Meerwin-Pondorf-Verley reagent (aluminum t-butoxide with another ketone) and N-bromosuccinimide

Then coupling of an organometallic carbon nucleophile, such as a Grignard reagent, an organolithium, lithium dialkylcopper or R⁶—SiMe₃ in TBAF with the ketone with the appropriate non-protic solvent at a suitable temperature, yields the 3′-C-branched sugar. The 3′-C-branched sugar can be optionally protected with a suitable protecting group, preferably with an acyl or silyl group, by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991.

The optionally protected sugar can then be coupled to the BASE by methods well known to those skilled in the art, as taught by Townsend Chemistry of Nucleosides and Nucleotides, Plenum Press, 1994. For example, an acylated sugar can be coupled to a silylated base with a lewis acid, such as tin tetrachloride, titanium tetrachloride or trimethylsilyltriflate in the appropriate solvent at a suitable temperature. Alternatively, a halo-sugar can be coupled to a silylated base with the presence of trimethylsilyltriflate.

Subsequently, the nucleoside can be deprotected by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991.

In a particular embodiment, the 3′-C-branched ribonucleoside is desired. The synthesis of a ribonucleoside is shown in Scheme 5. Alternatively, deoxyribo-nucleoside is desired. To obtain these nucleosides, the formed ribonucleoside can optionally be protected by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991, and then the 2′-OH can be reduced with a suitable reducing agent. Optionally, the 2′-hydroxyl can be activated to facilitate reduction; i.e. via the Barton reduction.

2. Modification of a Pre-Formed Nucleoside

The key starting material for this process is an appropriately substituted nucleoside with a 3′-OH and 3′-H. The nucleoside can be purchased or can be prepared by any known means including standard coupling techniques. The nucleoside can be optionally protected with suitable protecting groups, preferably with acyl or silyl groups, by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991.

The appropriately protected nucleoside can then be oxidized with the appropriate oxidizing agent in a compatible solvent at a suitable temperature to yield the 2′-modified sugar. Possible oxidizing agents are Jones reagent (a mixture of chromic acid and sulfuric acid), Collins's reagent (dipyridine Cr(VI) oxide, Corey's reagent (pyridinium chlorochromate), pyridinium dichromate, acid dichromate, potassium permanganate, MnO₂, ruthenium tetroxide, phase transfer catalysts such as chromic acid or permanganate supported on a polymer, Cl₂-pyridine, H₂O₂-ammonium molybdate, NaBrO₂—CAN, NaOCl in HOAc, copper chromite, copper oxide, Raney nickel, palladium acetate, Meerwin-Pondorf-Verley reagent (aluminum t-butoxide with another ketone) and N-bromosuccinimide.

Subsequently, the nucleoside can be deprotected by methods well known to those skilled in the art, as taught by GreeneGreene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991.

In a particular embodiment, the 3′-C-branched ribonucleoside is desired. The synthesis of a ribonucleoside is shown in Scheme 6. Alternatively, deoxyribo-nucleoside is desired. To obtain these nucleosides, the formed ribonucleoside can optionally be protected by methods well known to those skilled in the art, as taught by Greene et al. Protective Groups in Organic Synthesis, John Wiley and Sons, Second Edition, 1991, and then the 2′-OH can be reduced with a suitable reducing agent. Optionally, the 2′-hydroxyl can be activated to facilitate reduction; i.e. via the Barton reduction.

In another embodiment of the invention, the L-enantiomers are desired. Therefore, the L-enantiomers can be corresponding to the compounds of the invention can be prepared following the same foregoing general methods, beginning with the corresponding L-sugar or nucleoside L-enantiomer as starting material.

EXAMPLES Example 1 Preparation of 1′-C-methylriboadenine via 6-amino-9-(1-deoxy-β-D-psicofuranosyl)purine

As another alternative method of preparation, the title compound could also be prepared according to a published procedure (J. Farkas, and F. Sorm, “Nucleic acid components and their analogues. XCIV. Synthesis of 6-amino-9-(1-deoxy-β-D-psicofuranosyl)purine”, Collect. Czech. Chem. Commun. 1967, 32, 2663-2667. J. Farkas”, Collect. Czech. Chem. Commun. 1966, 31, 1535) (Scheme 7).

In a similar manner, but using the appropriate sugar and pyrimidine or purine bases, the following nucleosides of Formula I are prepared.

(I)

wherein: R¹ R² R³ X¹ X² Y H H H H H H H H H H H NH₂ H H H H H NH-cyclopropyl H H H H H NH-methyl H H H H H NH-ethyl H H H H H NH-acetyl H H H H H OH H H H H H OMe H H H H H OEt H H H H H O-cyclopropyl H H H H H O-acetyl H H H H H SH H H H H H SMe H H H H H SEt H H H H H S-cyclopropyl H H H H H F H H H H H Cl H H H H H Br H H H H H I monophosphate H H H H NH₂ monophosphate H H H H NH-acetyl monophosphate H H H H NH-cyclopropyl monophosphate H H H H NH-methyl monophosphate H H H H NH-ethyl monophosphate H H H H OH monophosphate H H H H O-acetyl monophosphate H H H H OMe monophosphate H H H H OEt monophosphate H H H H O-cyclopropyl monophosphate H H H H SH monophosphate H H H H SMe monophosphate H H H H SEt monophosphate H H H H S-cyclopropyl monophosphate H H H H F monophosphate H H H H Cl monophosphate H H H H Br monophosphate H H H H I diphosphate H H H H NH₂ diphosphate H H H H NH-acetyl diphosphate H H H H NH-cyclopropyl diphosphate H H H H NH-methyl diphosphate H H H H NH-ethyl diphosphate H H H H OH diphosphate H H H H O-acetyl diphosphate H H H H OMe diphosphate H H H H OEt diphosphate H H H H O-cyclopropyl diphosphate H H H H SH diphosphate H H H H SMe diphosphate H H H H SEt diphosphate H H H H S-cyclopropyl diphosphate H H H H F diphosphate H H H H Cl diphosphate H H H H Br diphosphate H H H H I triphosphate H H H H NH₂ triphosphate H H H H NH-acetyl triphosphate H H H H NH-cyclopropyl triphosphate H H H H NH-methyl triphosphate H H H H NH-ethyl triphosphate H H H H OH triphosphate H H H H OMe triphosphate H H H H OEt triphosphate H H H H O-cyclopropyl triphosphate H H H H O-acetyl triphosphate H H H H SH triphosphate H H H H SMe triphosphate H H H H SEt triphosphate H H H H S-cyclopropyl triphosphate H H H H F triphosphate H H H H Cl triphosphate H H H H Br triphosphate H H H H I monophosphate monophosphate monophosphate H H NH₂ monophosphate monophosphate monophosphate H H NH-cyclopropyl monophosphate monophosphate monophosphate H H OH monophosphate monophosphate monophosphate H H F monophosphate monophosphate monophosphate H H Cl diphosphate diphosphate diphosphate H H NH₂ diphosphate diphosphate diphosphate H H NH-cyclopropyl diphosphate diphosphate diphosphate H H OH diphosphate diphosphate diphosphate H H F diphosphate diphosphate diphosphate H H Cl triphosphate triphosphate triphosphate H H NH₂ triphosphate triphosphate triphosphate H H NH-cyclopropyl triphosphate triphosphate triphosphate H H OH triphosphate triphosphate triphosphate H H F triphosphate triphosphate triphosphate H H Cl H H H F H NH₂ H H H F H NH-cyclopropyl H H H F H OH H H H F H F H H H F H Cl H H H Cl H NH₂ H H H Cl H NH-cyclopropyl H H H Cl H OH H H H Cl H F H H H Cl H Cl H H H Br H NH₂ H H H Br H NH-cyclopropyl H H H Br H OH H H H Br H F H H H Br H Cl H H H NH₂ H NH₂ H H H NH₂ H NH-cyclopropyl H H H NH₂ H OH H H H NH₂ H F H H H NH₂ H Cl H H H SH H NH₂ H H H SH H NH-cyclopropyl H H H SH H OH H H H SH H F H H H SH H Cl acetyl H H H H NH₂ acetyl H H H H NH-cyclopropyl acetyl H H H H OH acetyl H H H H F acetyl H H H H Cl acetyl H H F H NH₂ acetyl H H F H NH-cyclopropyl acetyl H H F H OH acetyl H H F H F acetyl H H F H Cl H acetyl acetyl H H NH₂ H acetyl acetyl H H NH-cyclopropyl H acetyl acetyl H H OH H acetyl acetyl H H F H acetyl acetyl H H Cl acetyl acetyl acetyl H H NH₂ acetyl acetyl acetyl H H NH-cyclopropyl acetyl acetyl acetyl H H OH acetyl acetyl acetyl H H F acetyl acetyl acetyl H H Cl monophosphate acetyl acetyl H H NH₂ monophosphate acetyl acetyl H H NH-cyclopropyl monophosphate acetyl acetyl H H OH monophosphate acetyl acetyl H H F monophosphate acetyl acetyl H H Cl diphosphate acetyl acetyl H H NH₂ diphosphate acetyl acetyl H H NH-cyclopropyl diphosphate acetyl acetyl H H OH diphosphate acetyl acetyl H H F diphosphate acetyl acetyl H H Cl triphosphate acetyl acetyl H H NH₂ triphosphate acetyl acetyl H H NH-cyclopropyl triphosphate acetyl acetyl H H OH triphosphate acetyl acetyl H H F triphosphate acetyl acetyl H H Cl H H H H NH₂ H H H H H NH₂ NH₂ H H H H NH₂ NH-cyclopropyl H H H H NH₂ NH-methyl H H H H NH₂ NH-ethyl H H H H NH₂ NH-acetyl H H H H NH₂ OH H H H H NH₂ OMe H H H H NH₂ OEt H H H H NH₂ O-cyclopropyl H H H H NH₂ O-acetyl H H H H NH₂ SH H H H H NH₂ SMe H H H H NH₂ SEt H H H H NH₂ S-cyclopropyl H H H H NH₂ F H H H H NH₂ Cl H H H H NH₂ Br H H H H NH₂ I monophosphate H H H NH₂ NH₂ monophosphate H H H NH₂ NH-acetyl monophosphate H H H NH₂ NH-cyclopropyl monophosphate H H H NH₂ NH-methyl monophosphate H H H NH₂ NH-ethyl monophosphate H H H NH₂ OH monophosphate H H H NH₂ O-acetyl monophosphate H H H NH₂ OMe monophosphate H H H NH₂ OEt monophosphate H H H NH₂ O-cyclopropyl monophosphate H H H NH₂ SH monophosphate H H H NH₂ SMe monophosphate H H H NH₂ SEt monophosphate H H H NH₂ S-cyclopropyl monophosphate H H H NH₂ F monophosphate H H H NH₂ Cl monophosphate H H H NH₂ Br monophosphate H H H NH₂ I diphosphate H H H NH₂ NH₂ diphosphate H H H NH₂ NH-acetyl diphosphate H H H NH₂ NH-cyclopropyl diphosphate H H H NH₂ NH-methyl diphosphate H H H NH₂ NH-ethyl diphosphate H H H NH₂ OH diphosphate H H H NH₂ O-acetyl diphosphate H H H NH₂ OMe diphosphate H H H NH₂ OEt diphosphate H H H NH₂ O-cyclopropyl diphosphate H H H NH₂ SH diphosphate H H H NH₂ SMe diphosphate H H H NH₂ SEt diphosphate H H H NH₂ S-cyclopropyl diphosphate H H H NH₂ F diphosphate H H H NH₂ Cl diphosphate H H H NH₂ Br diphosphate H H H NH₂ I triphosphate H H H NH₂ NH₂ triphosphate H H H NH₂ NH-acetyl triphosphate H H H NH₂ NH-cyclopropyl triphosphate H H H NH₂ NH-methyl triphosphate H H H NH₂ NH-ethyl triphosphate H H H NH₂ OH triphosphate H H H NH₂ OMe triphosphate H H H NH₂ OEt triphosphate H H H NH₂ O-cyclopropyl triphosphate H H H NH₂ O-acetyl triphosphate H H H NH₂ SH triphosphate H H H NH₂ SMe triphosphate H H H NH₂ SEt triphosphate H H H NH₂ S-cyclopropyl triphosphate H H H NH₂ F triphosphate H H H NH₂ Cl triphosphate H H H NH₂ Br triphosphate H H H NH₂ I monophosphate monophosphate monophosphate H NH₂ NH₂ monophosphate monophosphate monophosphate H NH₂ NH-cyclopropyl monophosphate monophosphate monophosphate H NH₂ OH monophosphate monophosphate monophosphate H NH₂ F monophosphate monophosphate monophosphate H NH₂ Cl diphosphate diphosphate diphosphate H NH₂ NH₂ diphosphate diphosphate diphosphate H NH₂ NH-cyclopropyl diphosphate diphosphate diphosphate H NH₂ OH diphosphate diphosphate diphosphate H NH₂ F diphosphate diphosphate diphosphate H NH₂ Cl triphosphate triphosphate triphosphate H NH₂ NH₂ triphosphate triphosphate triphosphate H NH₂ NH-cyclopropyl triphosphate triphosphate triphosphate H NH₂ OH triphosphate triphosphate triphosphate H NH₂ F triphosphate triphosphate triphosphate H NH₂ Cl H H H F NH₂ NH₂ H H H F NH₂ NH-cyclopropyl H H H F NH₂ OH H H H F NH₂ F H H H F NH₂ Cl H H H Cl NH₂ NH₂ H H H Cl NH₂ NH-cyclopropyl H H H Cl NH₂ OH H H H Cl NH₂ F H H H Cl NH₂ Cl H H H Br NH₂ NH₂ H H H Br NH₂ NH-cyclopropyl H H H Br NH₂ OH H H H Br NH₂ F H H H Br NH₂ Cl H H H NH₂ NH₂ NH₂ H H H NH₂ NH₂ NH-cyclopropyl H H H NH₂ NH₂ OH H H H NH₂ NH₂ F H H H NH₂ NH₂ Cl H H H SH NH₂ NH₂ H H H SH NH₂ NH-cyclopropyl H H H SH NH₂ OH H H H SH NH₂ F H H H SH NH₂ Cl acetyl H H H NH₂ NH₂ acetyl H H H NH₂ NH-cyclopropyl acetyl H H H NH₂ OH acetyl H H H NH₂ F acetyl H H H NH₂ Cl acetyl H H F NH₂ NH₂ acetyl H H F NH₂ NH-cyclopropyl acetyl H H F NH₂ OH acetyl H H F NH₂ F acetyl H H F NH₂ Cl H acetyl acetyl H NH₂ NH₂ H acetyl acetyl H NH₂ NH-cyclopropyl H acetyl acetyl H NH₂ OH H acetyl acetyl H NH₂ F H acetyl acetyl H NH₂ Cl acetyl acetyl acetyl H NH₂ NH₂ acetyl acetyl acetyl H NH₂ NH-cyclopropyl acetyl acetyl acetyl H NH₂ OH acetyl acetyl acetyl H NH₂ F acetyl acetyl acetyl H NH₂ Cl monophosphate acetyl acetyl H NH₂ NH₂ monophosphate acetyl acetyl H NH₂ NH-cyclopropyl monophosphate acetyl acetyl H NH₂ OH monophosphate acetyl acetyl H NH₂ F monophosphate acetyl acetyl H NH₂ Cl diphosphate acetyl acetyl H NH₂ NH₂ diphosphate acetyl acetyl H NH₂ NH-cyclopropyl diphosphate acetyl acetyl H NH₂ OH diphosphate acetyl acetyl H NH₂ F diphosphate acetyl acetyl H NH₂ Cl triphosphate acetyl acetyl H NH₂ NH₂ triphosphate acetyl acetyl H NH₂ NH-cyclopropyl triphosphate acetyl acetyl H NH₂ OH triphosphate acetyl acetyl H NH₂ F triphosphate acetyl acetyl H NH₂ Cl H H H H Cl H H H H H Cl H H H H H Cl NH₂ H H H H Cl NH-cyclopropyl H H H H Cl NH-methyl H H H H Cl NH-ethyl H H H H Cl NH-acetyl H H H H Cl OH H H H H Cl OMe H H H H Cl OEt H H H H Cl O-cyclopropyl H H H H Cl O-acetyl H H H H Cl SH H H H H Cl SMe H H H H Cl SEt H H H H Cl S-cyclopropyl monophosphate H H H Cl NH₂ monophosphate H H H Cl NH-acetyl monophosphate H H H Cl NH-cyclopropyl monophosphate H H H Cl NH-methyl monophosphate H H H Cl NH-ethyl monophosphate H H H Cl OH monophosphate H H H Cl O-acetyl monophosphate H H H Cl OMe monophosphate H H H Cl OEt monophosphate H H H Cl O-cyclopropyl monophosphate H H H Cl SH monophosphate H H H Cl SMe monophosphate H H H Cl SEt monophosphate H H H Cl S-cyclopropyl diphosphate H H H Cl NH₂ diphosphate H H H Cl NH-acetyl diphosphate H H H Cl NH-cyclopropyl diphosphate H H H Cl NH-methyl diphosphate H H H Cl NH-ethyl diphosphate H H H Cl OH diphosphate H H H Cl O-acetyl diphosphate H H H Cl OMe diphosphate H H H Cl OEt diphosphate H H H Cl O-cyclopropyl diphosphate H H H Cl SH diphosphate H H H Cl SMe diphosphate H H H Cl SEt diphosphate H H H Cl S-cyclopropyl triphosphate H H H Cl NH₂ triphosphate H H H Cl NH-acetyl triphosphate H H H Cl NH-cyclopropyl triphosphate H H H Cl NH-methyl triphosphate H H H Cl NH-ethyl triphosphate H H H Cl OH triphosphate H H H Cl OMe triphosphate H H H Cl OEt triphosphate H H H Cl O-cyclopropyl triphosphate H H H Cl O-acetyl triphosphate H H H Cl SH triphosphate H H H Cl SMe triphosphate H H H Cl SEt triphosphate H H H Cl S-cyclopropyl monophosphate monophosphate monophosphate H Cl NH₂ monophosphate monophosphate monophosphate H Cl NH-cyclopropyl monophosphate monophosphate monophosphate H Cl OH diphosphate diphosphate diphosphate H Cl NH₂ diphosphate diphosphate diphosphate H Cl NH-cyclopropyl diphosphate diphosphate diphosphate H Cl OH triphosphate triphosphate triphosphate H Cl NH₂ triphosphate triphosphate triphosphate H Cl NH-cyclopropyl triphosphate triphosphate triphosphate H Cl OH H H H F Cl NH₂ H H H F Cl NH-cyclopropyl H H H F Cl OH H H H Cl Cl NH₂ H H H Cl Cl NH-cyclopropyl H H H Cl Cl OH H H H Br Cl NH₂ H H H Br Cl NH-cyclopropyl H H H Br Cl OH H H H NH₂ Cl NH₂ H H H NH₂ Cl NH-cyclopropyl H H H NH₂ Cl OH H H H SH Cl NH₂ H H H SH Cl NH-cyclopropyl H H H SH Cl OH acetyl H H H Cl NH₂ acetyl H H H Cl NH-cyclopropyl acetyl H H H Cl OH acetyl H H F Cl NH₂ acetyl H H F Cl NH-cyclopropyl acetyl H H F Cl OH H acetyl acetyl H Cl NH₂ H acetyl acetyl H Cl NH-cyclopropyl H acetyl acetyl H Cl OH acetyl acetyl acetyl H Cl NH₂ acetyl acetyl acetyl H Cl NH-cyclopropyl acetyl acetyl acetyl H Cl OH monophosphate acetyl acetyl H Cl NH₂ monophosphate acetyl acetyl H Cl NH-cyclopropyl monophosphate acetyl acetyl H Cl OH diphosphate acetyl acetyl H Cl NH₂ diphosphate acetyl acetyl H Cl NH-cyclopropyl diphosphate acetyl acetyl H Cl OH triphosphate acetyl acetyl H Cl NH₂ triphosphate acetyl acetyl H Cl NH-cyclopropyl triphosphate acetyl acetyl H Cl OH H H H H Cl NH₂ H H H H Cl NH-cyclopropyl H H H H Cl OH H H H H Br NH₂ H H H H Br NH-cyclopropyl H H H H Br OH

Alternatively, the following nucleosides of Formula IV are prepared, using the appropriate sugar and pyrimidine or purine bases.

(IV)

wherein: R¹ R² R³ X¹ Y H H H H H H H H H NH₂ H H H H NH-cyclopropyl H H H H NH-methyl H H H H NH-ethyl H H H H NH-acetyl H H H H OH H H H H OMe H H H H OEt H H H H O-cyclopropyl H H H H O-acetyl H H H H SH H H H H SMe H H H H SEt H H H H S-cyclopropyl monophosphate H H H NH₂ monophosphate H H H NH-acetyl monophosphate H H H NH-cyclopropyl monophosphate H H H NH-methyl monophosphate H H H NH-ethyl monophosphate H H H OH monophosphate H H H O-acetyl monophosphate H H H OMe monophosphate H H H OEt monophosphate H H H O-cyclopropyl monophosphate H H H SH monophosphate H H H SMe monophosphate H H H SEt monophosphate H H H S-cyclopropyl diphosphate H H H NH₂ diphosphate H H H NH-acetyl diphosphate H H H NH-cyclopropyl diphosphate H H H NH-methyl diphosphate H H H NH-ethyl diphosphate H H H OH diphosphate H H H O-acetyl diphosphate H H H OMe diphosphate H H H OEt diphosphate H H H O-cyclopropyl diphosphate H H H SH diphosphate H H H SMe diphosphate H H H SEt diphosphate H H H S-cyclopropyl triphosphate H H H NH₂ triphosphate H H H NH-acetyl triphosphate H H H NH-cyclopropyl triphosphate H H H NH-methyl triphosphate H H H NH-ethyl triphosphate H H H OH triphosphate H H H OMe triphosphate H H H OEt triphosphate H H H O-cyclopropyl triphosphate H H H O-acetyl triphosphate H H H SH triphosphate H H H SMe triphosphate H H H SEt triphosphate H H H S-cyclopropyl monophosphate monophosphate monophosphate H NH₂ monophosphate monophosphate monophosphate H NH-cyclopropyl monophosphate monophosphate monophosphate H OH diphosphate diphosphate diphosphate H NH₂ diphosphate diphosphate diphosphate H NH-cyclopropyl diphosphate diphosphate diphosphate H OH triphosphate triphosphate triphosphate H NH₂ triphosphate triphosphate triphosphate H NH-cyclopropyl triphosphate triphosphate triphosphate H OH H H H F NH₂ H H H F NH-cyclopropyl H H H F OH H H H Cl NH₂ H H H Cl NH-cyclopropyl H H H Cl OH H H H Br NH₂ H H H Br NH-cyclopropyl H H H Br OH H H H NH₂ NH₂ H H H NH₂ NH-cyclopropyl H H H NH₂ OH H H H SH NH₂ H H H SH NH-cyclopropyl H H H SH OH acetyl H H H NH₂ acetyl H H H NH-cyclopropyl acetyl H H H OH acetyl H H F NH₂ acetyl H H F NH-cyclopropyl acetyl H H F OH H acetyl acetyl H NH₂ H acetyl acetyl H NH-cyclopropyl H acetyl acetyl H OH acetyl acetyl acetyl H NH₂ acetyl acetyl acetyl H NH-cyclopropyl acetyl acetyl acetyl H OH monophosphate acetyl acetyl H NH₂ monophosphate acetyl acetyl H NH-cyclopropyl monophosphate acetyl acetyl H OH diphosphate acetyl acetyl H NH₂ diphosphate acetyl acetyl H NH-cyclopropyl diphosphate acetyl acetyl H OH triphosphate acetyl acetyl H NH₂ triphosphate acetyl acetyl H NH-cyclopropyl triphosphate acetyl acetyl H OH

Alternatively, the following nucleosides of Formula VII are prepared, using the appropriate sugar and pyrimidine or purine bases.

(VII)

wherein: R¹ R² R³ R⁶ X Base H H H CH₃ O 2,4-O- Diacetyluracil H H H CH₃ O Hypoxanthine H H H CH₃ O 2,4-O- Diacetylthymine H H H CH₃ O Thymine H H H CH₃ O Cytosine H H H CH₃ O 4-(N-mono- acetyl)cytosine H H H CH₃ O 4-(N,N- diacetyl)cytosine H H H CH₃ O Uracil H H H CH₃ O 5-Fluorouracil H H H CH₃ S 2,4-O- Diacetyluraci H H H CH₃ S Hypoxanthine H H H CH₃ S 2,4-O- Diacetylthymine H H H CH₃ S Thymine H H H CH₃ S Cytosine H H H CH₃ S 4-(N-mono- acetyl)cytosine H H H CH₃ S 4-(N,N- diacetyl)cytosine H H H CH₃ S Uracil H H H CH₃ S 5-Fluorouracil monophosphate H H CH₃ O 2,4-O- Diacetyluracil monophosphate H H CH₃ O Hypoxanthine monophosphate H H CH₃ O 2,4-O- Diacetylthym monophosphate H H CH₃ O Thymine monophosphate H H CH₃ O Cytosine monophosphate H H CH₃ O 4-(N-mono- acetyl)cytosine monophosphate H H CH₃ O 4-(N,N- diacetyl)cytosine monophosphate H H CH₃ O Uracil monophosphate H H CH₃ O 5-Fluorouracil monophosphate H H CH₃ S 2,4-O- Diacetyluracil monophosphate H H CH₃ S Hypoxanthine monophosphate H H CH₃ S 2,4-O- Diacetylthym monophosphate H H CH₃ S Thymine monophosphate H H CH₃ S Cytosine monophosphate H H CH₃ S 4-(N-mono- acetyl)cytosine monophosphate H H CH₃ S 4-(N,N- diacetyl)cytosine monophosphate H H CH₃ S Uracil monophosphate H H CH₃ S 5-Fluorouracil diphosphate H H CH₃ O 2,4-O- Diacetyluracil diphosphate H H CH₃ O Hypoxanthine diphosphate H H CH₃ O 2,4-O- Diacetylthymine diphosphate H H CH₃ O Thymine diphosphate H H CH₃ O Cytosine diphosphate H H CH₃ O 4-(N-mono- acetyl)cytosine diphosphate H H CH₃ O 4-(N,N- diacetyl)cytosine diphosphate H H CH₃ O Uracil diphosphate H H CH₃ O 5-Fluorouracil diphosphate H H CH₃ S 2,4-O- Diacetyluracil diphosphate H H CH₃ S Hypoxanthine diphosphate H H CH₃ S 2,4-O- Diacetylthym diphosphate H H CH₃ S Thymine diphosphate H H CH₃ S Cytosine triphosphate H H CH₃ O 2,4-O- Diacetyluracil triphosphate H H CH₃ O Hypoxanthine triphosphate H H CH₃ O 2,4-O- Diacetylthymine triphosphate H H CH₃ O Thymine triphosphate H H CH₃ O Cytosine triphosphate H H CH₃ O 4-(N-mono- acetyl)cytosine triphosphate H H CH₃ O 4-(N,N- diacetyl)cytosine triphosphate H H CH₃ O Uracil triphosphate H H CH₃ O 5-Fluorouracil triphosphate H H CH₃ S 2,4-O- Diacetyluracil triphosphate H H CH₃ S Hypoxanthine triphosphate H H CH₃ S 2,4-O- Diacetylthymine triphosphate H H CH₃ S Thymine triphosphate H H CH₃ S Cytosine monophosphate monophos- monophos- CF₃ O 2,4-O- phate phate Diacetyluracil monophosphate monophos- monophos- CF₃ O Hypoxanthine phate phate monophosphate monophos- monophos- CF₃ O 2,4-O- phate phate Diacetylthymine monophosphate monophos- monophos- CF₃ O Thymine phate phate monophosphate monophos- monophos- CF₃ O Cytosine phate phate monophosphate monophos- monophos- CF₃ O 4-(N-mono- phate phate acetyl)cytosine monophosphate monophos- monophos- CF₃ O 4-(N,N- phate phate diacetyl)cytosine monophosphate monophos- monophos- CF₃ O Uracil phate phate monophosphate monophos- monophos- CF₃ O 5-Fluorouracil phate phate monophosphate monophos- monophos- CF₃ S 2,4-O- phate phate Diacetyluracil monophosphate monophos- monophos- CF₃ S Hypoxanthine phate phate monophosphate monophos- monophos- CF₃ S 2,4-O- phate phate Diacetylthymine monophosphate monophos- monophos- CF₃ S Thymine phate phate monophosphate monophos- monophos- CF₃ S Cytosine phate phate monophosphate monophos- monophos- CF₃ S 4-(N-mono- phate phate acetyl)cytosine monophosphate monophos- monophos- CF₃ S 4-(N,N- phate phate diacetyl)cytosine monophosphate monophos- monophos- CF₃ S Uracil phate phate monophosphate monophos- monophos- CF₃ S 5-Fluorouracil phate phate acetyl acetyl acetyl CF₃ O 4-(N,N- diacetyl)cytosine acetyl acetyl acetyl CF₃ S 4-(N,N- diacetyl)cytosine acetyl acetyl acetyl 2- O 4-(N,N- bromo- diacetyl)cytosine vinyl acetyl acetyl acetyl 2- S 4-(N,N- bromo- diacetyl)cytosine vinyl H H H CH₃ O 2-(N,N-di- acetyl)guanine H H H CH₃ O 6-O-acetyl guanine H H H CH₃ O 8-fluoroguanine H H H CH₃ O guanine H H H CH₃ O 6-(N,N-di- acetyl)adenine H H H CH₃ O 2-fluoroadenine H H H CH₃ O 8-fluoroadenine H H H CH₃ O 2,8-difluoro- adenine H H H CH₃ O adenine H H H CH₃ S 2-(N,N-di- acetyl)guanine H H H CH₃ S 6-O-acetyl guanine H H H CH₃ S 8-fluoroguanine H H H CH₃ S guanine H H H CH₃ S 6-(N,N-di- acetyl)adenine H H H CH₃ S 2-fluoroadenine H H H CH₃ S 8-fluoroadenine H H H CH₃ S 2,8-difluoro- adenine H H H CH₃ S adenine monophosphate H H CH₃ O 2-(N,N-di- acetyl)guanine monophosphate H H CH₃ O 6-O-acetyl guanine monophosphate H H CH₃ O 8-fluoroguanine monophosphate H H CH₃ O guanine monophosphate H H CH₃ O 6-(N,N-di- acetyl)adenine monophosphate H H CH₃ O 2-fluoroadenine monophosphate H H CH₃ O 8-fluoroadenine monophosphate H H CH₃ O 2,8-difluoro- adenine monophosphate H H CH₃ O adenine monophosphate H H CH₃ S 2-(N,N-di- acetyl)guanine monophosphate H H CH₃ S 6-O-acetyl guanine monophosphate H H CH₃ S 8-fluoroguanine monophosphate H H CH₃ S guanine monophosphate H H CH₃ S 6-(N,N-di- acetyl)adenine monophosphate H H CH₃ S 2-fluoroadenine monophosphate H H CH₃ S 8-fluoroadenine monophosphate H H CH₃ S 2,8-difluoro- adenine monophosphate H H CH₃ S adenine diphosphate H H CH₃ O 2-(N,N-di- acetyl)guanine diphosphate H H CH₃ O 6-O-acetyl guanine diphosphate H H CH₃ O 8-fluoroguanine diphosphate H H CH₃ O guanine diphosphate H H CH₃ O 6-(N,N-di- acetyl)adenine diphosphate H H CH₃ O 2-fluoroadenine diphosphate H H CH₃ O 8-fluoroadenine diphosphate H H CH₃ O 2,8-difluoro- adenine diphosphate H H CH₃ O adenine diphosphate H H CH₃ S 2-(N,N-di- acetyl)guanine diphosphate H H CH₃ S 6-O-acetyl guanine diphosphate H H CH₃ S 8-fluoroguanine diphosphate H H CH₃ S guanine diphosphate H H CH₃ S 6-(N,N-di- acetyl)adenine diphosphate H H CH₃ S 2-fluoroadenine diphosphate H H CH₃ S 8-fluoroadenine diphosphate H H CH₃ S 2,8-difluoro- adenine diphosphate H H CH₃ S adenine triphosphate H H CH₃ O 2-(N,N-diacetyl)- guanine triphosphate H H CH₃ O 6-O-acetyl guanine triphosphate H H CH₃ O 8-fluoroguanine triphosphate H H CH₃ O guanine triphosphate H H CH₃ O 6-(N,N-di- acetyl)adenine triphosphate H H CH₃ O 2-fluoroadenine triphosphate H H CH₃ O 8-fluoroadenine triphosphate H H CH₃ O 2,8-difluoro- adenine triphosphate H H CH₃ O 2-(N,N-di- acetyl)guanine triphosphate H H CH₃ S 6-O-acetyl guanine triphosphate H H CH₃ S 8-fluoroguanine triphosphate H H CH₃ S guanine triphosphate H H CH₃ S 6-(N,N-di- acetyl)adenine triphosphate H H CH₃ S 2-fluoroadenine triphosphate H H CH₃ S 8-fluoroadenine triphosphate H H CH₃ S 2,8-difluoro- adenine triphosphate H H CH₃ S adenine monophosphate monophos- monophos- CF₃ O 2-(N,N-di- phate phate acetyl)guanine monophosphate monophos- monophos- CF₃ O 6-O-acetyl phate phate guanine monophosphate monophos- monophos- CF₃ O 8-fluoroguanine phate phate monophosphate monophos- monophos- CF₃ O guanine phate phate monophosphate monophos- monophos- CF₃ O 6-(N,N-di- phate phate acetyl)adenine monophosphate monophos- monophos- CF₃ O 2-fluoroadenine phate phate monophosphate monophos- monophos- CF₃ O 8-fluoroadenine phate phate monophosphate monophos- monophos- CF₃ O 2,8-difluoro- phate phate adenine monophosphate monophos- monophos- CF₃ O adenine phate phate monophosphate monophos- monophos- CF₃ S 2-(N,N-di- phate phate acetyl)guanine monophosphate monophos- monophos- CF₃ S 6-O-acetyl phate phate guanine monophosphate monophos- monophos- CF₃ S 8-fluoroguanine phate phate monophosphate monophos- monophos- CF₃ S guanine phate phate monophosphate monophos- monophos- CF₃ S 6-(N,N-di- phate phate acetyl)adenine monophosphate monophos- monophos- CF₃ S 2-fluoroadenine phate phate monophosphate monophos- monophos- CF₃ S 8-fluoroadenine phate phate monophosphate monophos- monophos- CF₃ S 2,8-difluoro- phate phate adenine monophosphate monophos- monophos- CF₃ S adenine phate phate acetyl acetyl acetyl CF₃ S guanine acetyl acetyl acetyl CF₃ S guanine acetyl acetyl acetyl 2- O guanine bromo- vinyl acetyl acetyl acetyl 2- S guanine bromo- vinyl

Alternatively, the following nucleosides of Formula VIII are prepared, using the appropriate sugar and pyrimidine or purine bases.

(VIII)

wherein R¹ R² R⁶ X Base H H CH₃ O 2,4-O-Diacetyluracil H H CH₃ O Hypoxanthine H H CH₃ O 2,4-O-Diacetylthymine H H CH₃ O Thymine H H CH₃ O Cytosine H H CH₃ O 4-(N-mono-acetyl)cytosine H H CH₃ O 4-(N,N-diacetyl)cytosine H H CH₃ O Uracil H H CH₃ O 5-Fluorouracil H H CH₃ S 2,4-O-Diacetyluracil H H CH₃ S Hypoxanthine H H CH₃ S 2,4-O-Diacetylthymine H H CH₃ S Thymine H H CH₃ S Cytosine H H CH₃ S 4-(N-mono-acetyl)cytosine H H CH₃ S 4-(N,N-diacetyl)cytosine H H CH₃ S Uracil H H CH₃ S 5-Fluorouracil monophosphate H CH₃ O 2,4-O-Diacetyluracil monophosphate H CH₃ O Hypoxanthine monophosphate H CH₃ O 2,4-O-Diacetylthymine monophosphate H CH₃ O Thymine monophosphate H CH₃ O Cytosine monophosphate H CH₃ O 4-(N-mono-acetyl)cytosine monophosphate H CH₃ O 4-(N,N-diacetyl)cytosine monophosphate H CH₃ O Uracil monophosphate H CH₃ O 5-Fluorouracil monophosphate H CH₃ S 2,4-O-Diacetyluracil monophosphate H CH₃ S Hypoxanthine monophosphate H CH₃ S 2,4-O-Diacetylthymine monophosphate H CH₃ S Thymine monophosphate H CH₃ S Cytosine monophosphate H CH₃ S 4-(N-mono-acetyl)cytosine monophosphate H CH₃ S 4-(N,N-diacetyl)cytosine monophosphate H CH₃ S Uracil monophosphate H CH₃ S 5-Fluorouracil diphosphate H CH₃ O 2,4-O-Diacetyluracil diphosphate H CH₃ O Hypoxanthine diphosphate H CH₃ O 2,4-O-Diacetylthymine diphosphate H CH₃ O Thymine diphosphate H CH₃ O Cytosine diphosphate H CH₃ O 4-(N-mono-acetyl)cytosine diphosphate H CH₃ O 4-(N,N-diacetyl)cytosine diphosphate H CH₃ O Uracil diphosphate H CH₃ O 5-Fluorouracil diphosphate H CH₃ S 2,4-O-Diacetyluracil diphosphate H CH₃ S Hypoxanthine diphosphate H CH₃ S 2,4-O-Diacetylthymine diphosphate H CH₃ S Thymine diphosphate H CH₃ S Cytosine diphosphate H CH₃ S 4-(N-mono-acetyl)cytosine diphosphate H CH₃ S 4-(N,N-diacetyl)cytosine diphosphate H CH₃ S Uracil diphosphate H CH₃ S 5-Fluorouracil triphosphate H CH₃ O 2,4-O-Diacetyluracil triphosphate H CH₃ O Hypoxanthine triphosphate H CH₃ O 2,4-O-Diacetylthymine triphosphate H CH₃ O Thymine triphosphate H CH₃ O Cytosine triphosphate H CH₃ O 4-(N-mono-acetyl)cytosine triphosphate H CH₃ O 4-(N,N-diacetyl)cytosine triphosphate H CH₃ O Uracil triphosphate H CH₃ O 5-Fluorouracil triphosphate H CH₃ S 2,4-O-Diacetyluracil triphosphate H CH₃ S Hypoxanthine triphosphate H CH₃ S 2,4-O-Diacetylthymine triphosphate H CH₃ S Thymine triphosphate H CH₃ S Cytosine triphosphate H CH₃ S 4-(N-mono-acetyl)cytosine triphosphate H CH₃ S 4-(N,N-diacetyl)cytosine triphosphate H CH₃ S Uracil triphosphate H CH₃ S 5-Fluorouracil monophosphate monophos- CF₃ O 2,4-O-Diacetyluracil phate monophosphate monophos- CF₃ O Hypoxanthine phate monophosphate monophos- CF₃ O 2,4-O-Diacetylthymine phate monophosphate monophos- CF₃ O Thymine phate monophosphate monophos- CF₃ O Cytosine phate monophosphate monophos- CF₃ O 4-(N-mono-acetyl)cytosine phate monophosphate monophos- CF₃ O 4-(N,N-diacetyl)cytosine phate monophosphate monophos- CF₃ O Uracil phate monophosphate monophos- CF₃ O 5-Fluorouracil phate monophosphate monophos- CF₃ S 2,4-O-Diacetyluracil phate monophosphate monophos- CF₃ S Hypoxanthine phate monophosphate monophos- CF₃ S 2,4-O-Diacetylthymine phate monophosphate monophos- CF₃ S Thymine phate monophosphate monophos- CF₃ S Cytosine phate monophosphate monophos- CF₃ S 4-(N-mono-acetyl)cytosine phate monophosphate monophos- CF₃ S 4-(N,N-diacetyl)cytosine phate monophosphate monophos- CF₃ S Uracil phate monophosphate monophos- CF₃ S 5-Fluorouracil phate acetyl acetyl CF₃ O 4-(N,N-diacetyl)cytosine acetyl acetyl CF₃ S 4-(N,N-diacetyl)cytosine acetyl acetyl 2-bromo- O 4-(N,N-diacetyl)cytosine vinyl acetyl acetyl 2-bromo- S 4-(N,N-diacetyl)cytosine vinyl H H CH₃ O 2-(N,N-diacetyl)-guanine H H CH₃ O 6-O-acetyl guanine H H CH₃ O 8-fluoroguanine H H CH₃ O guanine H H CH₃ O 6-(N,N-diacetyl)-adenine H H CH₃ O 2-fluoroadenine H H CH₃ O 8-fluoroadenine H H CH₃ O 2,8-difluoro-adenine H H CH₃ O adenine H H CH₃ S 2-(N,N-diacetyl)-guanine H H CH₃ S 6-O-acetyl guanine H H CH₃ S 8-fluoroguanine H H CH₃ S guanine H H CH₃ S 6-(N,N-diacetyl)-adenine H H CH₃ S 2-fluoroadenine H H CH₃ S 8-fluoroadenine H H CH₃ S 2,8-difluoro-adenine H H CH₃ S adenine monophosphate H CH₃ O 2-(N,N-diacetyl)-guanine monophosphate H CH₃ O 6-O-acetyl guanine monophosphate H CH₃ O 8-fluoroguanine monophosphate H CH₃ O guanine monophosphate H CH₃ O 6-(N,N-diacetyl)-adenine monophosphate H CH₃ O 2-fluoroadenine monophosphate H CH₃ O 8-fluoroadenine monophosphate H CH₃ O 2,8-difluoro-adenine monophosphate H CH₃ O adenine monophosphate H CH₃ S 2-(N,N-diacetyl)-guanine monophosphate H CH₃ S 6-O-acetyl guanine monophosphate H CH₃ S 8-fluoroguanine monophosphate H CH₃ S guanine monophosphate H CH₃ S 6-(N,N-diacetyl)-adenine monophosphate H CH₃ S 2-fluoroadenine monophosphate H CH₃ S 8-fluoroadenine monophosphate H CH₃ S 2,8-difluoro-adenine monophosphate H CH₃ S adenine diphosphate H CH₃ O 2-(N,N-diacetyl)-guanine diphosphate H CH₃ O 6-O-acetyl guanine diphosphate H CH₃ O 8-fluoroguanine diphosphate H CH₃ O guanine diphosphate H CH₃ O 6-(N,N-diacetyl)-adenine diphosphate H CH₃ O 2-fluoroadenine diphosphate H CH₃ O 8-fluoroadenine diphosphate H CH₃ O 2,8-difluoro-adenine diphosphate H CH₃ O adenine diphosphate H CH₃ S 2-(N,N-diacetyl)-guanine diphosphate H CH₃ S 6-O-acetyl guanine diphosphate H CH₃ S 8-fluoroguanine diphosphate H CH₃ S guanine diphosphate H CH₃ S 6-(N,N-diacetyl)-adenine diphosphate H CH₃ S 2-fluoroadenine diphosphate H CH₃ S 8-fluoroadenine diphosphate H CH₃ S 2,8-difluoro-adenine diphosphate H CH₃ S adenine triphosphate H CH₃ O 2-(N,N-diacetyl)-guanine triphosphate H CH₃ O 6-O-acetyl guanine triphosphate H CH₃ O 8-fluoroguanine triphosphate H CH₃ O guanine triphosphate H CH₃ O 6-(N,N-diacetyl)-adenine triphosphate H CH₃ O 2-fluoroadenine triphosphate H CH₃ O 8-fluoroadenine triphosphate H CH₃ O 2,8-difluoro-adenine triphosphate H CH₃ O adenine triphosphate H CH₃ S 2-(N,N-diacetyl)-guanine triphosphate H CH₃ S 6-O-acetyl guanine triphosphate H CH₃ S 8-fluoroguanine triphosphate H CH₃ S guanine triphosphate H CH₃ S 6-(N,N-diacetyl)-adenine triphosphate H CH₃ S 2-fluoroadenine triphosphate H CH₃ S 8-fluoroadenine triphosphate H CH₃ S 2,8-difluoro-adenine triphosphate H CH₃ S adenine monophosphate monophos- CF₃ O 2-(N,N-diacetyl)-guanine phate monophosphate monophos- CF₃ O 6-O-acetyl guanine phate monophosphate monophos- CF₃ O 8-fluoroguanine phate monophosphate monophos- CF₃ O guanine phate monophosphate monophos- CF₃ O 6-(N,N-diacetyl)-adenine phate monophosphate monophos- CF₃ O 2-fluoroadenine phate monophosphate monophos- CF₃ O 8-fluoroadenine phate monophosphate monophos- CF₃ O 2,8-difluoro-adenine phate monophosphate monophos- CF₃ O adenine phate monophosphate monophos- CF₃ S 2-(N,N-diacetyl)-guanine phate monophosphate monophos- CF₃ S 6-O-acetyl guanine phate monophosphate monophos- CF₃ S 8-fluoroguanine phate monophosphate monophos- CF₃ S guanine phate monophosphate monophos- CF₃ S 6-(N,N-diacetyl)-adenine phate monophosphate monophos- CF₃ S 2-fluoroadenine phate monophosphate monophos- CF₃ S 8-fluoroadenine phate monophosphate monophos- CF₃ S 2,8-difluoro-adenine phate monophosphate monophos- CF₃ S adenine phate acetyl acetyl CF₃ O guanine acetyl acetyl CF₃ S guanine acetyl acetyl 2-bromo- O guanine vinyl acetyl acetyl 2-bromo- S guanine vinyl

Alternatively, the following nucleosides of Formula IX are prepared, using the appropriate sugar and pyrimidine or purine bases.

(IX)

wherein: R¹ R⁶ X Base H CH₃ O 2,4-O-Diacetyluracil H CH₃ O Hypoxanthine H CH₃ O 2,4-O-Diacetylthymine H CH₃ O Thymine H CH₃ O Cytosine H CH₃ O 4-(N-mono-acetyl)cytosine H CH₃ O 4-(N,N-diacetyl)cytosine H CH₃ O Uracil H CH₃ O 5-Fluorouracil H CH₃ S 2,4-O-Diacetyluracil H CH₃ S Hypoxanthine H CH₃ S 2,4-O-Diacetylthymine H CH₃ S Thymine H CH₃ S Cytosine H CH₃ S 4-(N-mono-acetyl)cytosine H CH₃ S 4-(N,N-diacetyl)cytosine H CH₃ S Uracil H CH₃ S 5-Fluorouracil monophosphate CH₃ O 2,4-O-Diacetyluracil monophosphate CH₃ O Hypoxanthine monophosphate CH₃ O 2,4-O-Diacetylthymine monophosphate CH₃ O Thymine monophosphate CH₃ O Cytosine monophosphate CH₃ O 4-(N-mono-acetyl)cytosine monophosphate CH₃ O 4-(N,N-diacetyl)cytosine monophosphate CH₃ O Uracil monophosphate CH₃ O 5-Fluorouracil monophosphate CH₃ S 2,4-O-Diacetyluracil monophosphate CH₃ S Hypoxanthine monophosphate CH₃ S 2,4-O-Diacetylthymine monophosphate CH₃ S Thymine monophosphate CH₃ S Cytosine monophosphate CH₃ S 4-(N-mono-acetyl)cytosine monophosphate CH₃ S 4-(N,N-diacetyl)cytosine monophosphate CH₃ S Uracil monophosphate CH₃ S 5-Fluorouracil diphosphate CH₃ O 2,4-O-Diacetyluracil diphosphate CH₃ O Hypoxanthine diphosphate CH₃ O 2,4-O-Diacetylthymine diphosphate CH₃ O Thymine diphosphate CH₃ O Cytosine diphosphate CH₃ O 4-(N-mono-acetyl)cytosine diphosphate CH₃ O 4-(N,N-diacetyl)cytosine diphosphate CH₃ O Uracil diphosphate CH₃ O 5-Fluorouracil diphosphate CH₃ S 2,4-O-Diacetyluracil diphosphate CH₃ S Hypoxanthine diphosphate CH₃ S 2,4-O-Diacetylthymine diphosphate CH₃ S Thymine diphosphate CH₃ S Cytosine triphosphate CH₃ O 2,4-O-Diacetyluracil triphosphate CH₃ O Hypoxanthine triphosphate CH₃ O 2,4-O-Diacetylthymine triphosphate CH₃ O Thymine triphosphate CH₃ O Cytosine triphosphate CH₃ O 4-(N-mono-acetyl)cytosine triphosphate CH₃ O 4-(N,N-diacetyl)cytosine triphosphate CH₃ O Uracil triphosphate CH₃ O 5-Fluorouracil triphosphate CH₃ S 2,4-O-Diacetyluracil triphosphate CH₃ S Hypoxanthine triphosphate CH₃ S 2,4-O-Diacetylthymine triphosphate CH₃ S Thymine triphosphate CH₃ S Cytosine monophosphate CF₃ O 2,4-O-Diacetyluracil monophosphate CF₃ O Hypoxanthine monophosphate CF₃ O 2,4-O-Diacetylthymine monophosphate CF₃ O Thymine monophosphate CF₃ O Cytosine monophosphate CF₃ O 4-(N-mono-acetyl)cytosine monophosphate CF₃ O 4-(N,N-diacetyl)cytosine monophosphate CF₃ O Uracil monophosphate CF₃ O 5-Fluorouracil monophosphate CF₃ S 2,4-O-Diacetyluracil monophosphate CF₃ S Hypoxanthine monophosphate CF₃ S 2,4-O-Diacetylthymine monophosphate CF₃ S Thymine monophosphate CF₃ S Cytosine monophosphate CF₃ S 4-(N-mono-acetyl)cytosine monophosphate CF₃ S 4-(N,N-diacetyl)cytosine monophosphate CF₃ S Uracil monophosphate CF₃ S 5-Fluorouracil acetyl CF₃ O 4-(N,N-diacetyl)cytosine acetyl CF₃ S 4-(N,N-diacetyl)cytosine acetyl 2-bromo-vinyl O 4-(N,N-diacetyl)cytosine acetyl 2-bromo-vinyl S 4-(N,N-diacetyl)cytosine

Alternatively, the following nucleosides of Formula XVI are prepared, using the appropriate sugar and pyrimidine or purine bases.

(XVI)

wherein: R¹ R⁶ R⁷ R⁸ X Base R¹⁰ R⁹ H CH₃ H H O 2,4-O-Diacetyluracil OH Me H CH₃ H H O Hypoxanthine OH Me H CH₃ H H O 2,4-O-Diacetylthymine OH Me H CH₃ H H O Thymine OH Me H CH₃ H H O Cytosine OH Me H CH₃ H H O 4-(N-mono-acetyl)cytosine OH Me H CH₃ H H O 4-(N,N-diacetyl)cytosine OH Me H CH₃ H H O Uracil OH Me H CH₃ H H O 5-Fluorouracil OH Me H CH₃ H H S 2,4-O-Diacetyluracil OH Me H CH₃ H H S Hypoxanthine OH Me H CH₃ H H S 2,4-O-Diacetylthymine OH Me H CH₃ H H S Thymine OH Me H CH₃ H H S Cytosine OH Me H CH₃ H H S 4-(N-mono-acetyl)cytosine OH Me H CH₃ H H S 4-(N,N-diacetyl)cytosine OH Me H CH₃ H H S Uracil OH Me H CH₃ H H S 5-Fluorouracil OH Me monophosphate CH₃ H H O 2,4-O-Diacetyluracil OH Me monophosphate CH₃ H H O Hypoxanthine OH Me monophosphate CH₃ H H O 2,4-O-Diacetylthymine OH Me monophosphate CH₃ H H O Thymine OH Me monophosphate CH₃ H H O Cytosine OH Me monophosphate CH₃ H H O 4-(N-mono-acetyl)cytosine OH Me monophosphate CH₃ H H O 4-(N,N-diacetyl)cytosine OH Me monophosphate CH₃ H H O Uracil OH Me monophosphate CH₃ H H O 5-Fluorouracil OH Me monophosphate CH₃ H H S 2,4-O-Diacetyluracil OH Me monophosphate CH₃ H H S Hypoxanthine OH Me monophosphate CH₃ H H S 2,4-O-Diacetylthymine OH Me monophosphate CH₃ H H S Thymine OH Me monophosphate CH₃ H H S Cytosine OH Me monophosphate CH₃ H H S 4-(N-mono-acetyl)cytosine OH Me monophosphate CH₃ H H S 4-(N,N-diacetyl)cytosine OH Me monophosphate CH₃ H H S Uracil OH Me monophosphate CH₃ H H S 5-Fluorouracil OH Me diphosphate CH₃ H H O 2,4-O-Diacetyluracil OH Me diphosphate CH₃ H H O Hypoxanthine OH Me diphosphate CH₃ H H O 2,4-O-Diacetylthymine OH Me diphosphate CH₃ H H O Thymine OH Me diphosphate CH₃ H H O Cytosine OH Me diphosphate CH₃ H H O 4-(N-mono-acetyl)cytosine OH Me diphosphate CH₃ H H O 4-(N,N-diacetyl)cytosine OH Me diphosphate CH₃ H H O Uracil OH Me diphosphate CH₃ H H O 5-Fluorouracil OH Me diphosphate CH₃ H H S 2,4-O-Diacetyluracil OH Me diphosphate CH₃ H H S Hypoxanthine OH Me diphosphate CH₃ H H S 2,4-O-Diacetylthymine OH Me diphosphate CH₃ H H S Thymine OH Me diphosphate CH₃ H H S Cytosine OH Me triphosphate CH₃ H H O 2,4-O-Diacetyluracil OH Me triphosphate CH₃ H H O Hypoxanthine OH Me triphosphate CH₃ H H O 2,4-O-Diacetylthymine OH Me triphosphate CH₃ H H O Thymine OH Me triphosphate CH₃ H H O Cytosine OH Me triphosphate CH₃ H H O 4-(N-mono-acetyl)cytosine OH Me triphosphate CH₃ H H O 4-(N,N-diacetyl)cytosine OH Me triphosphate CH₃ H H O Uracil OH Me triphosphate CH₃ H H O 5-Fluorouracil OH Me triphosphate CH₃ H H S 2,4-O-Diacetyluracil OH Me triphosphate CH₃ H H S Hypoxanthine OH Me triphosphate CH₃ H H S 2,4-O-Diacetylthymine OH Me triphosphate CH₃ H H S Thymine OH Me triphosphate CH₃ H H S Cytosine OH Me monophosphate CF₃ H H O 2,4-O-Diacetyluracil OH Me monophosphate CF₃ H H O Hypoxanthine OH Me monophosphate CF₃ H H O 2,4-O-Diacetylthymine OH Me monophosphate CF₃ H H O Thymine OH Me monophosphate CF₃ H H O Cytosine OH Me monophosphate CF₃ H H O 4-(N-mono-acetyl)cytosine OH Me monophosphate CF₃ H H O 4-(N,N-diacetyl)cytosine OH Me monophosphate CF₃ H H O Uracil OH Me monophosphate CF₃ H H O 5-Fluorouracil OH Me monophosphate CF₃ H H S 2,4-O-Diacetyluracil OH Me monophosphate CF₃ H H S Hypoxanthine OH Me monophosphate CF₃ H H S 2,4-O-Diacetylthymine OH Me monophosphate CF₃ H H S Thymine OH Me monophosphate CF₃ H H S Cytosine OH Me monophosphate CF₃ H H S 4-(N-mono-acetyl)cytosine OH Me monophosphate CF₃ H H S 4-(N,N-diacetyl)cytosine OH Me monophosphate CF₃ H H S Uracil OH Me monophosphate CF₃ H H S 5-Fluorouracil OH Me acetyl CH₃ H H O 4-(N,N-diacetyl)cytosine H Br acetyl CH₃ H H S 4-(N,N-diacetyl)cytosine H Br acetyl CH₃ OH H O 4-(N,N-diacetyl)cytosine H Br acetyl CH₃ OH H S 4-(N,N-diacetyl)cytosine H Br

Example 2 Preparation of 2′-C-methylriboadenine

The title compound was prepared according to a published procedure (R. E. Harry-O'kuru, J. M. Smith, and M. S. Wolfe, “A short, flexible route toward 2′-C-branched ribonucleosides”, J. Org. Chem. 1997, 62, 1754-1759) (Scheme 8).

In a similar manner, but using the appropriate sugar and pyrimidine or purine bases, the following nucleosides of Formula II are prepared.

(II)

wherein: R¹ R² R³ X¹ X² Y H H H H H H H H H H H NH₂ H H H H H NH-cyclopropyl H H H H H NH-methyl H H H H H NH-ethyl H H H H H NH-acetyl H H H H H OH H H H H H OMe H H H H H OEt H H H H H O-cyclopropyl H H H H H O-acetyl H H H H H SH H H H H H SMe H H H H H SEt H H H H H S-cyclopropyl H H H H H F H H H H H Cl H H H H H Br H H H H H I monophosphate H H H H NH₂ monophosphate H H H H NH-acetyl monophosphate H H H H NH-cyclopropyl monophosphate H H H H NH-methyl monophosphate H H H H NH-ethyl monophosphate H H H H OH monophosphate H H H H O-acetyl monophosphate H H H H OMe monophosphate H H H H OEt monophosphate H H H H O-cyclopropyl monophosphate H H H H SH monophosphate H H H H SMe monophosphate H H H H SEt monophosphate H H H H S-cyclopropyl monophosphate H H H H F monophosphate H H H H Cl monophosphate H H H H Br monophosphate H H H H I diphosphate H H H H NH₂ diphosphate H H H H NH-acetyl diphosphate H H H H NH-cyclopropyl diphosphate H H H H NH-methyl diphosphate H H H H NH-ethyl diphosphate H H H H OH diphosphate H H H H O-acetyl diphosphate H H H H OMe diphosphate H H H H OEt diphosphate H H H H O-cyclopropyl diphosphate H H H H SH diphosphate H H H H SMe diphosphate H H H H SEt diphosphate H H H H S-cyclopropyl diphosphate H H H H F diphosphate H H H H Cl diphosphate H H H H Br diphosphate H H H H I triphosphate H H H H NH₂ triphosphate H H H H NH-acetyl triphosphate H H H H NH-cyclopropyl triphosphate H H H H NH-methyl triphosphate H H H H NH-ethyl triphosphate H H H H OH triphosphate H H H H OMe triphosphate H H H H OEt triphosphate H H H H O-cyclopropyl triphosphate H H H H O-acetyl triphosphate H H H H SH triphosphate H H H H SMe triphosphate H H H H SEt triphosphate H H H H S-cyclopropyl triphosphate H H H H F triphosphate H H H H Cl triphosphate H H H H Br triphosphate H H H H I monophosphate monophosphate monophosphate H H NH₂ monophosphate monophosphate monophosphate H H NH-cyclopropyl monophosphate monophosphate monophosphate H H OH monophosphate monophosphate monophosphate H H F monophosphate monophosphate monophosphate H H Cl diphosphate diphosphate diphosphate H H NH₂ diphosphate diphosphate diphosphate H H NH-cyclopropyl diphosphate diphosphate diphosphate H H OH diphosphate diphosphate diphosphate H H F diphosphate diphosphate diphosphate H H Cl triphosphate triphosphate triphosphate H H NH₂ triphosphate triphosphate triphosphate H H NH-cyclopropyl triphosphate triphosphate triphosphate H H OH triphosphate triphosphate triphosphate H H F triphosphate triphosphate triphosphate H H Cl H H H F H NH₂ H H H F H NH-cyclopropyl H H H F H OH H H H F H F H H H F H Cl H H H Cl H NH₂ H H H Cl H NH-cyclopropyl H H H Cl H OH H H H Cl H F H H H Cl H Cl H H H Br H NH₂ H H H Br H NH-cyclopropyl H H H Br H OH H H H Br H F H H H Br H Cl H H H NH₂ H NH₂ H H H NH₂ H NH-cyclopropyl H H H NH₂ H OH H H H NH₂ H F H H H NH₂ H Cl H H H SH H NH₂ H H H SH H NH-cyclopropyl H H H SH H OH H H H SH H F H H H SH H Cl acetyl H H H H NH₂ acetyl H H H H NH-cyclopropyl acetyl H H H H OH acetyl H H H H F acetyl H H H H Cl acetyl H H F H NH₂ acetyl H H F H NH-cyclopropyl acetyl H H F H OH acetyl H H F H F acetyl H H F H Cl H acetyl acetyl H H NH₂ H acetyl acetyl H H NH-cyclopropyl H acetyl acetyl H H OH H acetyl acetyl H H F H acetyl acetyl H H Cl acetyl acetyl acetyl H H NH₂ acetyl acetyl acetyl H H NH-cyclopropyl acetyl acetyl acetyl H H OH acetyl acetyl acetyl H H F acetyl acetyl acetyl H H Cl monophosphate acetyl acetyl H H NH₂ monophosphate acetyl acetyl H H NH-cyclopropyl monophosphate acetyl acetyl H H OH monophosphate acetyl acetyl H H F monophosphate acetyl acetyl H H Cl diphosphate acetyl acetyl H H NH₂ diphosphate acetyl acetyl H H NH-cyclopropyl diphosphate acetyl acetyl H H OH diphosphate acetyl acetyl H H F diphosphate acetyl acetyl H H Cl triphosphate acetyl acetyl H H NH₂ triphosphate acetyl acetyl H H NH-cyclopropyl triphosphate acetyl acetyl H H OH triphosphate acetyl acetyl H H F triphosphate acetyl acetyl H H Cl H H H H NH₂ H H H H H NH₂ NH₂ H H H H NH₂ NH-cyclopropyl H H H H NH₂ NH-methyl H H H H NH₂ NH-ethyl H H H H NH₂ NH-acetyl H H H H NH₂ OH H H H H NH₂ OMe H H H H NH₂ OEt H H H H NH₂ O-cyclopropyl H H H H NH₂ O-acetyl H H H H NH₂ SH H H H H NH₂ SMe H H H H NH₂ SEt H H H H NH₂ S-cyclopropyl H H H H NH₂ F H H H H NH₂ Cl H H H H NH₂ Br H H H H NH₂ I monophosphate H H H NH₂ NH₂ monophosphate H H H NH₂ NH-acetyl monophosphate H H H NH₂ NH-cyclopropyl monophosphate H H H NH₂ NH-methyl monophosphate H H H NH₂ NH-ethyl monophosphate H H H NH₂ OH monophosphate H H H NH₂ O-acetyl monophosphate H H H NH₂ OMe monophosphate H H H NH₂ OEt monophosphate H H H NH₂ O-cyclopropyl monophosphate H H H NH₂ SH monophosphate H H H NH₂ SMe monophosphate H H H NH₂ SEt monophosphate H H H NH₂ S-cyclopropyl monophosphate H H H NH₂ F monophosphate H H H NH₂ Cl monophosphate H H H NH₂ Br monophosphate H H H NH₂ I diphosphate H H H NH₂ NH₂ diphosphate H H H NH₂ NH-acetyl diphosphate H H H NH₂ NH-cyclopropyl diphosphate H H H NH₂ NH-methyl diphosphate H H H NH₂ NH-ethyl diphosphate H H H NH₂ OH diphosphate H H H NH₂ O-acetyl diphosphate H H H NH₂ OMe diphosphate H H H NH₂ OEt diphosphate H H H NH₂ O-cyclopropyl diphosphate H H H NH₂ SH diphosphate H H H NH₂ SMe diphosphate H H H NH₂ SEt diphosphate H H H NH₂ S-cyclopropyl diphosphate H H H NH₂ F diphosphate H H H NH₂ Cl diphosphate H H H NH₂ Br diphosphate H H H NH₂ I triphosphate H H H NH₂ NH₂ triphosphate H H H NH₂ NH-acetyl triphosphate H H H NH₂ NH-cyclopropyl triphosphate H H H NH₂ NH-methyl triphosphate H H H NH₂ NH-ethyl triphosphate H H H NH₂ OH triphosphate H H H NH₂ OMe triphosphate H H H NH₂ OEt triphosphate H H H NH₂ O-cyclopropyl triphosphate H H H NH₂ O-acetyl triphosphate H H H NH₂ SH triphosphate H H H NH₂ SMe triphosphate H H H NH₂ SEt triphosphate H H H NH₂ S-cyclopropyl triphosphate H H H NH₂ F triphosphate H H H NH₂ Cl triphosphate H H H NH₂ Br triphosphate H H H NH₂ I monophosphate monophosphate monophosphate H NH₂ NH₂ monophosphate monophosphate monophosphate H NH₂ NH-cyclopropyl monophosphate monophosphate monophosphate H NH₂ OH monophosphate monophosphate monophosphate H NH₂ F monophosphate monophosphate monophosphate H NH₂ Cl diphosphate diphosphate diphosphate H NH₂ NH₂ diphosphate diphosphate diphosphate H NH₂ NH-cyclopropyl diphosphate diphosphate diphosphate H NH₂ OH diphosphate diphosphate diphosphate H NH₂ F diphosphate diphosphate diphosphate H NH₂ Cl triphosphate triphosphate triphosphate H NH₂ NH₂ triphosphate triphosphate triphosphate H NH₂ NH-cyclopropyl triphosphate triphosphate triphosphate H NH₂ OH triphosphate triphosphate triphosphate H NH₂ F triphosphate triphosphate triphosphate H NH₂ Cl H H H F NH₂ NH₂ H H H F NH₂ NH-cyclopropyl H H H F NH₂ OH H H H F NH₂ F H H H F NH₂ Cl H H H Cl NH₂ NH₂ H H H Cl NH₂ NH-cyclopropyl H H H Cl NH₂ OH H H H Cl NH₂ F H H H Cl NH₂ Cl H H H Br NH₂ NH₂ H H H Br NH₂ NH-cyclopropyl H H H Br NH₂ OH H H H Br NH₂ F H H H Br NH₂ Cl H H H NH₂ NH₂ NH₂ H H H NH₂ NH₂ NH-cyclopropyl H H H NH₂ NH₂ OH H H H NH₂ NH₂ F H H H NH₂ NH₂ Cl H H H SH NH₂ NH₂ H H H SH NH₂ NH-cyclopropyl H H H SH NH₂ OH H H H SH NH₂ F H H H SH NH₂ Cl acetyl H H H NH₂ NH₂ acetyl H H H NH₂ NH-cyclopropyl acetyl H H H NH₂ OH acetyl H H H NH₂ F acetyl H H H NH₂ Cl acetyl H H F NH₂ NH₂ acetyl H H F NH₂ NH-cyclopropyl acetyl H H F NH₂ OH acetyl H H F NH₂ F acetyl H H F NH₂ Cl H acetyl acetyl H NH₂ NH₂ H acetyl acetyl H NH₂ NH-cyclopropyl H acetyl acetyl H NH₂ OH H acetyl acetyl H NH₂ F H acetyl acetyl H NH₂ Cl acetyl acetyl acetyl H NH₂ NH₂ acetyl acetyl acetyl H NH₂ NH-cyclopropyl acetyl acetyl acetyl H NH₂ OH acetyl acetyl acetyl H NH₂ F acetyl acetyl acetyl H NH₂ Cl monophosphate acetyl acetyl H NH₂ NH₂ monophosphate acetyl acetyl H NH₂ NH-cyclopropyl monophosphate acetyl acetyl H NH₂ OH monophosphate acetyl acetyl H NH₂ F monophosphate acetyl acetyl H NH₂ Cl diphosphate acetyl acetyl H NH₂ NH₂ diphosphate acetyl acetyl H NH₂ NH-cyclopropyl diphosphate acetyl acetyl H NH₂ OH diphosphate acetyl acetyl H NH₂ F diphosphate acetyl acetyl H NH₂ Cl triphosphate acetyl acetyl H NH₂ NH₂ triphosphate acetyl acetyl H NH₂ NH-cyclopropyl triphosphate acetyl acetyl H NH₂ OH triphosphate acetyl acetyl H NH₂ F triphosphate acetyl acetyl H NH₂ Cl H H H H Cl H H H H H Cl H H H H H Cl NH₂ H H H H Cl NH-cyclopropyl H H H H Cl NH-methyl H H H H Cl NH-ethyl H H H H Cl NH-acetyl H H H H Cl OH H H H H Cl OMe H H H H Cl OEt H H H H Cl O-cyclopropyl H H H H Cl O-acetyl H H H H Cl SH H H H H Cl SMe H H H H Cl SEt H H H H Cl S-cyclopropyl monophosphate H H H Cl NH₂ monophosphate H H H Cl NH-acetyl monophosphate H H H Cl NH-cyclopropyl monophosphate H H H Cl NH-methyl monophosphate H H H Cl NH-ethyl monophosphate H H H Cl OH monophosphate H H H Cl O-acetyl monophosphate H H H Cl OMe monophosphate H H H Cl OEt monophosphate H H H Cl O-cyclopropyl monophosphate H H H Cl SH monophosphate H H H Cl SMe monophosphate H H H Cl SEt monophosphate H H H Cl S-cyclopropyl diphosphate H H H Cl NH₂ diphosphate H H H Cl NH-acetyl diphosphate H H H Cl NH-cyclopropyl diphosphate H H H Cl NH-methyl diphosphate H H H Cl NH-ethyl diphosphate H H H Cl OH diphosphate H H H Cl O-acetyl diphosphate H H H Cl OMe diphosphate H H H Cl OEt diphosphate H H H Cl O-cyclopropyl diphosphate H H H Cl SH diphosphate H H H Cl SMe diphosphate H H H Cl SEt diphosphate H H H Cl S-cyclopropyl triphosphate H H H Cl NH₂ triphosphate H H H Cl NH-acetyl triphosphate H H H Cl NH-cyclopropyl triphosphate H H H Cl NH-methyl triphosphate H H H Cl NH-ethyl triphosphate H H H Cl OH triphosphate H H H Cl OMe triphosphate H H H Cl OEt triphosphate H H H Cl O-cyclopropyl triphosphate H H H Cl O-acetyl triphosphate H H H Cl SH triphosphate H H H Cl SMe triphosphate H H H Cl SEt triphosphate H H H Cl S-cyclopropyl monophosphate monophosphate monophosphate H Cl NH₂ monophosphate monophosphate monophosphate H Cl NH-cyclopropyl monophosphate monophosphate monophosphate H Cl OH diphosphate diphosphate diphosphate H Cl NH₂ diphosphate diphosphate diphosphate H Cl NH-cyclopropyl diphosphate diphosphate diphosphate H Cl OH triphosphate triphosphate triphosphate H Cl NH₂ triphosphate triphosphate triphosphate H Cl NH-cyclopropyl triphosphate triphosphate triphosphate H Cl OH H H H F Cl NH₂ H H H F Cl NH-cyclopropyl H H H F Cl OH H H H Cl Cl NH₂ H H H Cl Cl NH-cyclopropyl H H H Cl Cl OH H H H Br Cl NH₂ H H H Br Cl NH-cyclopropyl H H H Br Cl OH H H H NH₂ Cl NH₂ H H H NH₂ Cl NH-cyclopropyl H H H NH₂ Cl OH H H H SH Cl NH₂ H H H SH Cl NH-cyclopropyl H H H SH Cl OH acetyl H H H Cl NH₂ acetyl H H H Cl NH-cyclopropyl acetyl H H H Cl OH acetyl H H F Cl NH₂ acetyl H H F Cl NH-cyclopropyl acetyl H H F Cl OH H acetyl acetyl H Cl NH₂ H acetyl acetyl H Cl NH-cyclopropyl H acetyl acetyl H Cl OH acetyl acetyl acetyl H Cl NH₂ acetyl acetyl acetyl H Cl NH-cyclopropyl acetyl acetyl acetyl H Cl OH monophosphate acetyl acetyl H Cl NH₂ monophosphate acetyl acetyl H Cl NH-cyclopropyl monophosphate acetyl acetyl H Cl OH diphosphate acetyl acetyl H Cl NH₂ diphosphate acetyl acetyl H Cl NH-cyclopropyl diphosphate acetyl acetyl H Cl OH triphosphate acetyl acetyl H Cl NH₂ triphosphate acetyl acetyl H Cl NH-cyclopropyl triphosphate acetyl acetyl H Cl OH H H H H Cl NH₂ H H H H Cl NH-cyclopropyl H H H H Cl OH H H H H Br NH₂ H H H H Br NH-cyclopropyl H H H H Br OH

Alternatively, the following nucleosides of Formula V are prepared, using the appropriate sugar and pyrimidine or purine bases.

(V)

wherein: R¹ R² R³ X¹ Y H H H H H H H H H NH₂ H H H H NH-cyclopropyl H H H H NH-methyl H H H H NH-ethyl H H H H NH-acetyl H H H H OH H H H H OMe H H H H OEt H H H H O-cyclopropyl H H H H O-acetyl H H H H SH H H H H SMe H H H H SEt H H H H S-cyclopropyl monophosphate H H H NH₂ monophosphate H H H NH-acetyl monophosphate H H H NH-cyclopropyl monophosphate H H H NH-methyl monophosphate H H H NH-ethyl monophosphate H H H OH monophosphate H H H O-acetyl monophosphate H H H OMe monophosphate H H H OEt monophosphate H H H O-cyclopropyl monophosphate H H H SH monophosphate H H H SMe monophosphate H H H SEt monophosphate H H H S-cyclopropyl diphosphate H H H NH₂ diphosphate H H H NH-acetyl diphosphate H H H NH-cyclopropyl diphosphate H H H NH-methyl diphosphate H H H NH-ethyl diphosphate H H H OH diphosphate H H H O-acetyl diphosphate H H H OMe diphosphate H H H OEt diphosphate H H H O-cyclopropyl diphosphate H H H SH diphosphate H H H SMe diphosphate H H H SEt diphosphate H H H S-cyclopropyl triphosphate H H H NH₂ triphosphate H H H NH-acetyl triphosphate H H H NH-cyclopropyl triphosphate H H H NH-methyl triphosphate H H H NH-ethyl triphosphate H H H OH triphosphate H H H OMe triphosphate H H H OEt triphosphate H H H O-cyclopropyl triphosphate H H H O-acetyl triphosphate H H H SH triphosphate H H H SMe triphosphate H H H SEt triphosphate H H H S-cyclopropyl monophosphate monophosphate monophosphate H NH₂ monophosphate monophosphate monophosphate H NH-cyclopropyl monophosphate monophosphate monophosphate H OH diphosphate diphosphate diphosphate H NH₂ diphosphate diphosphate diphosphate H NH-cyclopropyl diphosphate diphosphate diphosphate H OH triphosphate triphosphate triphosphate H NH₂ triphosphate triphosphate triphosphate H NH-cyclopropyl triphosphate triphosphate triphosphate H OH H H H F NH₂ H H H F NH-cyclopropyl H H H F OH H H H Cl NH₂ H H H Cl NH-cyclopropyl H H H Cl OH H H H Br NH₂ H H H Br NH-cyclopropyl H H H Br OH H H H NH₂ NH₂ H H H NH₂ NH-cyclopropyl H H H NH₂ OH H H H SH NH₂ H H H SH NH-cyclopropyl H H H SH OH acetyl H H H NH₂ acetyl H H H NH-cyclopropyl acetyl H H H OH acetyl H H F NH₂ acetyl H H F NH-cyclopropyl acetyl H H F OH H acetyl acetyl H NH₂ H acetyl acetyl H NH-cyclopropyl H acetyl acetyl H OH acetyl acetyl acetyl H NH₂ acetyl acetyl acetyl H NH-cyclopropyl acetyl acetyl acetyl H OH monophosphate acetyl acetyl H NH₂ monophosphate acetyl acetyl H NH-cyclopropyl monophosphate acetyl acetyl H OH diphosphate acetyl acetyl H NH₂ diphosphate acetyl acetyl H NH-cyclopropyl diphosphate acetyl acetyl H OH triphosphate acetyl acetyl H NH₂ triphosphate acetyl acetyl H NH-cyclopropyl triphosphate acetyl acetyl H OH

Alternatively, the following nucleosides of Formula X are prepared, using the appropriate sugar and pyrimidine or purine bases.

(X)

wherein: R¹ R² R³ R⁶ X Base H H H CH₃ O 2,4-O-Diacetyluracil H H H CH₃ O Hypoxanthine H H H CH₃ O 2,4-O-Diacetylthymine H H H CH₃ O Thymine H H H CH₃ O Cytosine H H H CH₃ O 4-(N-mono-acetyl)cytosine H H H CH₃ O 4-(N,N-diacetyl)cytosine H H H CH₃ O Uracil H H H CH₃ O 5-Fluorouracil H H H CH₃ S 2,4-O-Diacetyluraci H H H CH₃ S Hypoxanthine H H H CH₃ S 2,4-O-Diacetylthymine H H H CH₃ S Thymine H H H CH₃ S Cytosine H H H CH₃ S 4-(N-mono-acetyl)cytosine H H H CH₃ S 4-(N,N-diacetyl)cytosine H H H CH₃ S Uracil H H H CH₃ S 5-Fluorouracil monophosphate H H CH₃ O 2,4-O-Diacetyluracil monophosphate H H CH₃ O Hypoxanthine monophosphate H H CH₃ O 2,4-O-Diacetylthym monophosphate H H CH₃ O Thymine monophosphate H H CH₃ O Cytosine monophosphate H H CH₃ O 4-(N-mono-acetyl)cytosine monophosphate H H CH₃ O 4-(N,N-diacetyl)cytosine monophosphate H H CH₃ O Uracil monophosphate H H CH₃ O 5-Fluorouracil monophosphate H H CH₃ S 2,4-O-Diacetyluracil monophosphate H H CH₃ S Hypoxanthine monophosphate H H CH₃ S 2,4-O-Diacetylthym monophosphate H H CH₃ S Thymine monophosphate H H CH₃ S Cytosine monophosphate H H CH₃ S 4-(N-mono-acetyl)cytosine monophosphate H H CH₃ S 4-(N,N-diacetyl)cytosine monophosphate H H CH₃ S Uracil monophosphate H H CH₃ S 5-Fluorouracil diphosphate H H CH₃ O 2,4-O-Diacetyluracil diphosphate H H CH₃ O Hypoxanthine diphosphate H H CH₃ O 2,4-O-Diacetylthymine diphosphate H H CH₃ O Thymine diphosphate H H CH₃ O Cytosine diphosphate H H CH₃ O 4-(N-mono-acetyl)cytosine diphosphate H H CH₃ O 4-(N,N-diacetyl)cytosine diphosphate H H CH₃ O Uracil diphosphate H H CH₃ O 5-Fluorouracil diphosphate H H CH₃ S 2,4-O-Diacetyluracil diphosphate H H CH₃ S Hypoxanthine diphosphate H H CH₃ S 2,4-O-Diacetylthym diphosphate H H CH₃ S Thymine diphosphate H H CH₃ S Cytosine triphosphate H H CH₃ O 2,4-O-Diacetyluracil triphosphate H H CH₃ O Hypoxanthine triphosphate H H CH₃ O 2,4-O-Diacetylthymine triphosphate H H CH₃ O Thymine triphosphate H H CH₃ O Cytosine triphosphate H H CH₃ O 4-(N-mono-acetyl)cytosine triphosphate H H CH₃ O 4-(N,N-diacetyl)cytosine triphosphate H H CH₃ O Uracil triphosphate H H CH₃ O 5-Fluorouracil triphosphate H H CH₃ S 2,4-O-Diacetyluracil triphosphate H H CH₃ S Hypoxanthine triphosphate H H CH₃ S 2,4-O-Diacetylthymine triphosphate H H CH₃ S Thymine triphosphate H H CH₃ S Cytosine monophosphate monophosphate monophosphate CF₃ O 2,4-O-Diacetyluracil monophosphate monophosphate monophosphate CF₃ O Hypoxanthine monophosphate monophosphate monophosphate CF₃ O 2,4-O-Diacetylthymine monophosphate monophosphate monophosphate CF₃ O Thymine monophosphate monophosphate monophosphate CF₃ O Cytosine monophosphate monophosphate monophosphate CF₃ O 4-(N-mono-acetyl)cytosine monophosphate monophosphate monophosphate CF₃ O 4-(N,N-diacetyl)cytosine monophosphate monophosphate monophosphate CF₃ O Uracil monophosphate monophosphate monophosphate CF₃ O 5-Fluorouracil monophosphate monophosphate monophosphate CF₃ S 2,4-O-Diacetyluracil monophosphate monophosphate monophosphate CF₃ S Hypoxanthine monophosphate monophosphate monophosphate CF₃ S 2,4-O-Diacetylthymine monophosphate monophosphate monophosphate CF₃ S Thymine monophosphate monophosphate monophosphate CF₃ S Cytosine monophosphate monophosphate monophosphate CF₃ S 4-(N-mono-acetyl)cytosine monophosphate monophosphate monophosphate CF₃ S 4-(N,N-diacetyl)cytosine monophosphate monophosphate monophosphate CF₃ S Uracil monophosphate monophosphate monophosphate CF₃ S 5-Fluorouracil acetyl acetyl acetyl CF₃ O 4-(N,N-diacetyl)cytosine acetyl acetyl acetyl CF₃ S 4-(N,N-diacetyl)cytosine acetyl acetyl acetyl 2-bromo-vinyl O 4-(N,N-diacetyl)cytosine acetyl acetyl acetyl 2-bromo-vinyl S 4-(N,N-diacetyl)cytosine H H H CH₃ O 2-(N,N-diacetyl)-guanine H H H CH₃ O 6-O-acetyl guanine H H H CH₃ O 8-fluoroguanine H H H CH₃ O guanine H H H CH₃ O 6-(N,N-diacetyl)-adenine H H H CH₃ O 2-fluoroadenine H H H CH₃ O 8-fluoroadenine H H H CH₃ O 2,8-difluoro-adenine H H H CH₃ O adenine H H H CH₃ S 2-(N,N-diacetyl)-guanine H H H CH₃ S 6-O-acetyl guanine H H H CH₃ S 8-fluoroguanine H H H CH₃ S guanine H H H CH₃ S 6-(N,N-diacetyl)-adenine H H H CH₃ S 2-fluoroadenine H H H CH₃ S 8-fluoroadenine H H H CH₃ S 2,8-difluoro-adenine H H H CH₃ S adenine monophosphate H H CH₃ O 2-(N,N-diacetyl)-guanine monophosphate H H CH₃ O 6-O-acetyl guanine monophosphate H H CH₃ O 8-fluoroguanine monophosphate H H CH₃ O guanine monophosphate H H CH₃ O 6-(N,N-diacetyl)-adenine monophosphate H H CH₃ O 2-fluoroadenine monophosphate H H CH₃ O 8-fluoroadenine monophosphate H H CH₃ O 2,8-difluoro-adenine monophosphate H H CH₃ O adenine monophosphate H H CH₃ S 2-(N,N-diacetyl)-guanine monophosphate H H CH₃ S 6-O-acetyl guanine monophosphate H H CH₃ S 8-fluoroguanine monophosphate H H CH₃ S guanine monophosphate H H CH₃ S 6-(N,N-diacetyl)-adenine monophosphate H H CH₃ S 2-fluoroadenine monophosphate H H CH₃ S 8-fluoroadenine monophosphate H H CH₃ S 2,8-difluoro-adenine monophosphate H H CH₃ S adenine diphosphate H H CH₃ O 2-(N,N-diacetyl)-guanine diphosphate H H CH₃ O 6-O-acetyl guanine diphosphate H H CH₃ O 8-fluoroguanine diphosphate H H CH₃ O guanine diphosphate H H CH₃ O 6-(N,N-diacetyl)-adenine diphosphate H H CH₃ O 2-fluoroadenine diphosphate H H CH₃ O 8-fluoroadenine diphosphate H H CH₃ O 2,8-difluoro-adenine diphosphate H H CH₃ O adenine diphosphate H H CH₃ S 2-(N,N-diacetyl)-guanine diphosphate H H CH₃ S 6-O-acetyl guanine diphosphate H H CH₃ S 8-fluoroguanine diphosphate H H CH₃ S guanine diphosphate H H CH₃ S 6-(N,N-diacetyl)-adenine diphosphate H H CH₃ S 2-fluoroadenine diphosphate H H CH₃ S 8-fluoroadenine diphosphate H H CH₃ S 2,8-difluoro-adenine diphosphate H H CH₃ S adenine triphosphate H H CH₃ O 2-(N,N-diacetyl)-guanine triphosphate H H CH₃ O 6-O-acetyl guanine triphosphate H H CH₃ O 8-fluoroguanine triphosphate H H CH₃ O guanine triphosphate H H CH₃ O 6-(N,N-diacetyl)-adenine triphosphate H H CH₃ O 2-fluoroadenine triphosphate H H CH₃ O 8-fluoroadenine triphosphate H H CH₃ O 2,8-difluoro-adenine triphosphate H H CH₃ O 2-(N,N-diacetyl)-guanine triphosphate H H CH₃ S 6-O-acetyl guanine triphosphate H H CH₃ S 8-fluoroguanine triphosphate H H CH₃ S guanine triphosphate H H CH₃ S 6-(N,N-diacetyl)-adenine triphosphate H H CH₃ S 2-fluoroadenine triphosphate H H CH₃ S 8-fluoroadenine triphosphate H H CH₃ S 2,8-difluoro-adenine triphosphate H H CH₃ S adenine monophosphate monophosphate monophosphate CF₃ O 2-(N,N-diacetyl)-guanine monophosphate monophosphate monophosphate CF₃ O 6-O-acetyl guanine monophosphate monophosphate monophosphate CF₃ O 8-fluoroguanine monophosphate monophosphate monophosphate CF₃ O guanine monophosphate monophosphate monophosphate CF₃ O 6-(N,N-diacetyl)-adenine monophosphate monophosphate monophosphate CF₃ O 2-fluoroadenine monophosphate monophosphate monophosphate CF₃ O 8-fluoroadenine monophosphate monophosphate monophosphate CF₃ O 2,8-difluoro-adenine monophosphate monophosphate monophosphate CF₃ O adenine monophosphate monophosphate monophosphate CF₃ S 2-(N,N-diacetyl)-guanine monophosphate monophosphate monophosphate CF₃ S 6-O-acetyl guanine monophosphate monophosphate monophosphate CF₃ S 8-fluoroguanine monophosphate monophosphate monophosphate CF₃ S guanine monophosphate monophosphate monophosphate CF₃ S 6-(N,N-diacetyl)-adenine monophosphate monophosphate monophosphate CF₃ S 2-fluoroadenine monophosphate monophosphate monophosphate CF₃ S 8-fluoroadenine monophosphate monophosphate monophosphate CF₃ S 2,8-difluoro-adenine monophosphate monophosphate monophosphate CF₃ S adenine acetyl acetyl acetyl CF₃ O guanine acetyl acetyl acetyl CF₃ S guanine acetyl acetyl acetyl 2-bromo-vinyl O guanine acetyl acetyl acetyl 2-bromo-vinyl S guanine

Alternatively, the following nucleosides of Formula XI are prepared, using the appropriate sugar and pyrimidine or purine bases.

(XI)

wherein: R¹ R² R⁷ R⁶ X Base H H H CH₃ O 2,4-O- Diacetyluracil H H H CH₃ O Hypoxanthine H H H CH₃ O 2,4-O- Diacetylthymine H H H CH₃ O Thymine H H H CH₃ O Cytosine H H H CH₃ O 4-(N-mono- acetyl)cytosine H H H CH₃ O 4-(N,N- diacetyl)cytosine H H H CH₃ O Uracil H H H CH₃ O 5-Fluorouracil H H H CH₃ S 2,4-O- Diacetyluracil H H H CH₃ S Hypoxanthine H H H CH₃ S 2,4-O- Diacetylthymine H H H CH₃ S Thymine H H H CH₃ S Cytosine H H H CH₃ S 4-(N-mono- acetyl)cytosin H H H CH₃ S 4-(N,N- diacetyl)cytosine H H H CH₃ S Uracil H H H CH₃ S 5-Fluorouracil CH₃ monophosphate H H CH₃ O 2,4-O- Diacetyluracil monophosphate H H CH₃ O Hypoxanthine monophosphate H H CH₃ O 2,4-O- Diacetylthymine monophosphate H H CH₃ O Thymine monophosphate H H CH₃ O Cytosine monophosphate H H CH₃ O 4-(N-mono- acetyl)cytosine monophosphate H H CH₃ O 4-(N,N- diacetyl)cytosine monophosphate H H CH₃ O Uracil monophosphate H H CH₃ O 5-Fluorouracil monophosphate H H CH₃ S 2,4-O- Diacetyluracil monophosphate H H CH₃ S Hypoxanthine monophosphate H H CH₃ S 2,4-O- Diacetylthymine monophosphate H H CH₃ S Thymine monophosphate H H CH₃ S Cytosine monophosphate H H CH₃ S 4-(N-mono- acetyl)cytosine monophosphate H H CH₃ S 4-(N,N- diacetyl)cytosine monophosphate H H CH₃ S Uracil monophosphate H H CH₃ S 5-Fluorouracil diphosphate H H CH₃ O 2,4-O-Diacetylurac diphosphate H H CH₃ O Hypoxanthine diphosphate H H CH₃ O 2,4-O- Diacetylthymine diphosphate H H CH₃ O Thymine diphosphate H H CH₃ O Cytosine diphosphate H H CH₃ O 4-(N-mono- acetyl)cytosine diphosphate H H CH₃ O 4-(N,N- diacetyl)cytosine diphosphate H H CH₃ O Uracil diphosphate H H CH₃ O 5-Fluorouracil diphosphate H H CH₃ S 2,4-O- Diacetyluracil diphosphate H H CH₃ S Hypoxanthine diphosphate H H CH₃ S 2,4-O- Diacetylthym diphosphate H H CH₃ S Thymine diphosphate H H CH₃ S Cytosine triphosphate H H CH₃ O 2,4-O- Diacetyluracil triphosphate H H CH₃ O Hypoxanthine triphosphate H H CH₃ O 2,4-O- Diacetylthymine triphosphate H H CH₃ O Thymine triphosphate H H CH₃ O Cytosine triphosphate H H CH₃ O 4-(N-mono- acetyl)cytosine triphosphate H H CH₃ O 4-(N,N- diacetyl)cytos triphosphate H H CH₃ O Uracil triphosphate H H CH₃ O 5-Fluorouracil triphosphate H H CH₃ S 2,4-O- Diacetyluracil triphosphate H H CH₃ S Hypoxanthine triphosphate H H CH₃ S 2,4-O- Diacetylthym triphosphate H H CH₃ S Thymine triphosphate H H CH₃ S Cytosine monophosphate monophosphate Br CF₃ O 2,4-O- Diacetyluracil monophosphate monophosphate Br CF₃ O Hypoxanthine monophosphate monophosphate Br CF₃ O 2,4-O- Diacetylthymine monophosphate monophosphate Br CF₃ O Thymine monophosphate monophosphate Br CF₃ O Cytosine monophosphate monophosphate Br CF₃ O 4-(N-mono- acetyl)cytosine monophosphate monophosphate Br CF₃ O 4-(N,N- diacetyl)cytosine monophosphate monophosphate Br CF₃ O Uracil monophosphate monophosphate Br CF₃ O 5-Fluorouracil monophosphate monophosphate Br CF₃ S 2,4-O- Diacetyluracil monophosphate monophosphate Br CF₃ S Hypoxanthine monophosphate monophosphate Br CF₃ S 2,4-O- Diacetylthymine monophosphate monophosphate Br CF₃ S Thymine monophosphate monophosphate Br CF₃ S Cytosine monophosphate monophosphate Br CF₃ S 4-(N-mono- acetyl)cytosine monophosphate monophosphate Br CF₃ S 4-(N,N- diacetyl)cytos monophosphate monophosphate Br CF₃ S Uracil monophosphate monophosphate Br CF₃ S 5-Fluorouracil acetyl acetyl NO2 CF₃ O 4-(N,N- diacetyl)cytosine acetyl acetyl NO2 CF₃ S 4-(N,N- diacetyl)cytosine acetyl acetyl NO2 CF₃ O 4-(N,N- diacetyl)cytosine acetyl acetyl NO2 2- S 4-(N,N- bromo- diacetyl)cytosine vinyl

Alternatively, the following nucleosides of Formula XII are prepared, using the appropriate sugar and pyrimidine or purine bases.

(XII)

wherein: R¹ R⁶ X Base H CH₃ O 2,4-O-Diacetyluracil H CH₃ O Hypoxanthine H CH₃ O 2,4-O-Diacetylthymine H CH₃ O Thymine H CH₃ O Cytosine H CH₃ O 4-(N-mono-acetyl)cytosine H CH₃ O 4-(N,N-diacetyl)cytosine H CH₃ O Uracil H CH₃ O 5-Fluorouracil H CH₃ S 2,4-O-Diacetyluracil H CH₃ S Hypoxanthine H CH₃ S 2,4-O-Diacetylthymine H CH₃ S Thymine H CH₃ S Cytosine H CH₃ S 4-(N-mono-acetyl)cytosine H CH₃ S 4-(N,N-diacetyl)cytosine H CH₃ S Uracil H CH₃ S 5-Fluorouracil monophosphate CH₃ O 2,4-O-Diacetyluracil monophosphate CH₃ O Hypoxanthine monophosphate CH₃ O 2,4-O-Diacetylthymine monophosphate CH₃ O Thymine monophosphate CH₃ O Cytosine monophosphate CH₃ O 4-(N-mono-acetyl)cytosine monophosphate CH₃ O 4-(N,N-diacetyl)cytosine monophosphate CH₃ O Uracil monophosphate CH₃ O 5-Fluorouracil monophosphate CH₃ S 2,4-O-Diacetyluracil monophosphate CH₃ S Hypoxanthine monophosphate CH₃ S 2,4-O-Diacetylthymine monophosphate CH₃ S Thymine monophosphate CH₃ S Cytosine monophosphate CH₃ S 4-(N-mono-acetyl)cytosine monophosphate CH₃ S 4-(N,N-diacetyl)cytosine monophosphate CH₃ S Uracil monophosphate CH₃ S 5-Fluorouracil diphosphate CH₃ O 2,4-O-Diacetyluracil diphosphate CH₃ O Hypoxanthine diphosphate CH₃ O 2,4-O-Diacetylthymine diphosphate CH₃ O Thymine diphosphate CH₃ O Cytosine diphosphate CH₃ O 4-(N-mono-acetyl)cytosine diphosphate CH₃ O 4-(N,N-diacetyl)cytosine diphosphate CH₃ O Uracil diphosphate CH₃ O 5-Fluorouracil diphosphate CH₃ S 2,4-O-Diacetyluracil diphosphate CH₃ S Hypoxanthine diphosphate CH₃ S 2,4-O-Diacetylthymine diphosphate CH₃ S Thymine diphosphate CH₃ S Cytosine triphosphate CH₃ O 2,4-O-Diacetyluracil triphosphate CH₃ O Hypoxanthine triphosphate CH₃ O 2,4-O-Diacetylthymine triphosphate CH₃ O Thymine triphosphate CH₃ O Cytosine triphosphate CH₃ O 4-(N-mono-acetyl)cytosine triphosphate CH₃ O 4-(N,N-diacetyl)cytosine triphosphate CH₃ O Uracil triphosphate CH₃ O 5-Fluorouracil triphosphate CH₃ S 2,4-O-Diacetyluracil triphosphate CH₃ S Hypoxanthine triphosphate CH₃ S 2,4-O-Diacetylthymine triphosphate CH₃ S Thymine triphosphate CH₃ S Cytosine monophosphate CF₃ O 2,4-O-Diacetyluracil monophosphate CF₃ O Hypoxanthine monophosphate CF₃ O 2,4-O-Diacetylthymine monophosphate CF₃ O Thymine monophosphate CF₃ O Cytosine monophosphate CF₃ O 4-(N-mono-acetyl)cytosine monophosphate CF₃ O 4-(N,N-diacetyl)cytosine monophosphate CF₃ O Uracil monophosphate CF₃ O 5-Fluorouracil monophosphate CF₃ S 2,4-O-Diacetyluracil monophosphate CF₃ S Hypoxanthine monophosphate CF₃ S 2,4-O-Diacetylthymine monophosphate CF₃ S Thymine monophosphate CF₃ S Cytosine monophosphate CF₃ S 4-(N-mono-acetyl)cytosine monophosphate CF₃ S 4-(N,N-diacetyl)cytosine monophosphate CF₃ S Uracil monophosphate CF₃ S 5-Fluorouracil acetyl CF₃ O 4-(N,N-diacetyl)cytosine acetyl CF₃ S 4-(N,N-diacetyl)cytosine acetyl 2-bromo-vinyl O 4-(N,N-diacetyl)cytosine Acetyl 2-bromo-vinyl S 4-(N,N-diacetyl)cytosine

Alternatively, the following nucleosides of Formula XVII are prepared, using the appropriate sugar and pyrimidine or purine bases.

(XVII)

wherein: R¹ R⁶ R⁷ X Base R⁹ R¹⁰ H CH₃ H O 2,4-O-Diacetyluracil NHAc Me H CH₃ H O Hypoxanthine NH2 Me H CH₃ H O 2,4-O-Diacetylthymine NHAc Me H CH₃ H O Thymine NH2 Me H CH₃ H O Cytosine NH2 Me H CH₃ H O 4-(N-mono-acetyl)cytosine NHAc Me H CH₃ H O 4-(N,N-diacetyl)cytosine NHAc Me H CH₃ H O Uracil NH2 Me H CH₃ H O 5-Fluorouracil NH2 Me H CH₃ H S 2,4-O-Diacetyluracil NHAc Me H CH₃ H S Hypoxanthine NH2 Me H CH₃ H S 2,4-O-Diacetylthymine NHAc Me H CH₃ H S Thymine NH2 Me H CH₃ H S Cytosine NH2 Me H CH₃ H S 4-(N-mono-acetyl)cytosine NHAc Me H CH₃ H S 4-(N,N-diacetyl)cytosine NHAc Me H CH₃ H S Uracil NH2 Me H CH₃ H S 5-Fluorouracil NH2 Me monophosphate CH₃ H O 2,4-O-Diacetyluracil NHAc Me monophosphate CH₃ H O Hypoxanthine NH2 Me monophosphate CH₃ H O 2,4-O-Diacetylthymine NHAc Me monophosphate CH₃ H O Thymine NH2 Me monophosphate CH₃ H O Cytosine NH2 Me monophosphate CH₃ H O 4-(N-mono-acetyl)cytosine NHAc Me monophosphate CH₃ H O 4-(N,N-diacetyl)cytosine NHAc Me monophosphate CH₃ H O Uracil NH2 Me monophosphate CH₃ H O 5-Fluorouracil NH2 Me monophosphate CH₃ H S 2,4-O-Diacetyluracil NHAc Me monophosphate CH₃ H S Hypoxanthine NH2 Me monophosphate CH₃ H S 2,4-O-Diacetylthymine NHAc Me monophosphate CH₃ H S Thymine NH2 Me monophosphate CH₃ H S Cytosine NH2 Me monophosphate CH₃ H S 4-(N-mono-acetyl)cytosine NHAc Me monophosphate CH₃ H S 4-(N,N-diacetyl)cytosine NHAc Me monophosphate CH₃ H S Uracil NH2 Me monophosphate CH₃ H S 5-Fluorouracil NH2 Me diphosphate CH₃ H O 2,4-O-Diacetyluracil NHAc Me diphosphate CH₃ H O Hypoxanthine NH2 Me diphosphate CH₃ H O 2,4-O-Diacetylthymine NH2 Me diphosphate CH₃ H O Thymine NH2 Me diphosphate CH₃ H O Cytosine NH2 Me diphosphate CH₃ H O 4-(N-mono-acetyl)cytosine NHAc Me diphosphate CH₃ H O 4-(N,N-diacetyl)cytos NHAc Me diphosphate CH₃ H O Uracil NH2 Me diphosphate CH₃ H O 5-Fluorouracil NH2 Me diphosphate CH₃ H S 2,4-O-Diacetyluracil NH2 Me diphosphate CH₃ H S Hypoxanthine NH2 Me diphosphate CH₃ H S 2,4-O-Diacetylthymine NHAc Me diphosphate CH₃ H S Thymine NH2 Me diphosphate CH₃ H S Cytosine NH2 Me triphosphate CH₃ H O 2,4-O-Diacetyluracil NHAc Me triphosphate CH₃ H O Hypoxanthine NHAc Me triphosphate CH₃ H O 2,4-O-Diacetylthymine NHAc Me triphosphate CH₃ H O Thymine NH2 Me triphosphate CH₃ H O Cytosine NH2 Me triphosphate CH₃ H O 4-(N-mono-acetyl)cytosine NHAc Me triphosphate CH₃ H O 4-(N,N-diacetyl)cytosine NH2 Me triphosphate CH₃ H O Uracil NH2 Me triphosphate CH₃ H O 5-Fluorouracil NH2 Me triphosphate CH₃ H S 2,4-O-Diacetyluracil NH2 Me triphosphate CH₃ H S Hypoxanthine NH2 Me triphosphate CH₃ H S 2,4-O-Diacetylthymine NH2 Me triphosphate CH₃ H S Thymine NH2 Me triphosphate CH₃ H S Cytosine NH2 Me monophosphate CF₃ H O 2,4-O-Diacetyluracil NH2 Me monophosphate CF₃ H O Hypoxanthine NH2 Me monophosphate CF₃ H O 2,4-O-Diacetylthymine NH2 Me monophosphate CF₃ H O Thymine NH2 Me monophosphate CF₃ H O Cytosine NH2 Me monophosphate CF₃ H O 4-(N-mono-acetyl)cytosine NH2 Me monophosphate CF₃ H O 4-(N,N-diacetyl)cytosine NH2 Me monophosphate CF₃ H O Uracil NH2 Me monophosphate CF₃ H O 5-Fluorouracil NH2 Me monophosphate CF₃ H S 2,4-O-Diacetyluracil NH2 Me monophosphate CF₃ H S Hypoxanthine NH2 Me monophosphate CF₃ H S 2,4-O-Diacetylthymine NH2 Me monophosphate CF₃ H S Thymine NH2 Me monophosphate CF₃ H S Cytosine NH2 Me monophosphate CF₃ H S 4-(N-mono-acetyl)cytosine NH2 Me monophosphate CF₃ H S 4-(N,N-diacetyl)cytosine NH2 Me monophosphate CF₃ H S Uracil NH2 Me monophosphate CF₃ H S 5-Fluorouracil NH2 Me acetyl CH₃ H O 4-(N,N-diacetyl)cytosine H Br acetyl CH₃ H S 4-(N,N-diacetyl)cytosine H Br acetyl CH₃ OH O 4-(N,N-diacetyl)cytosine H Br acetyl CH₃ OH S 4-(N,N-diacetyl)cytosine H Br

Example 3 Preparation of 3′-C-methylriboadenine

The title compound can be prepared according to a published procedure (R. F. Nutt, M. J. Dickinson, F. W. Holly, and E. Walton, “Branched-chain sugar nucleosides. III. 3′-C-methyladenine”, J. Org. Chem. 1968, 33, 1789-1795) (Scheme 9).

In a similar manner, but using the appropriate sugar and pyrimidine or purine bases, the following nucleosides of Formula III are prepared.

(III)

wherein: R¹ R² R³ X¹ X² Y H H H H H H H H H H H NH₂ H H H H H NH-cyclopropyl H H H H H NH-methyl H H H H H NH-ethyl H H H H H NH-acetyl H H H H H OH H H H H H OMe H H H H H OEt H H H H H O-cyclopropyl H H H H H O-acetyl H H H H H SH H H H H H SMe H H H H H SEt H H H H H S-cyclopropyl H H H H H F H H H H H Cl H H H H H Br H H H H H I monophosphate H H H H NH₂ monophosphate H H H H NH-acetyl monophosphate H H H H NH-cyclopropyl monophosphate H H H H NH-methyl monophosphate H H H H NH-ethyl monophosphate H H H H OH monophosphate H H H H O-acetyl monophosphate H H H H OMe monophosphate H H H H OEt monophosphate H H H H O-cyclopropyl monophosphate H H H H SH monophosphate H H H H SMe monophosphate H H H H SEt monophosphate H H H H S-cyclopropyl monophosphate H H H H F monophosphate H H H H Cl monophosphate H H H H Br monophosphate H H H H I diphosphate H H H H NH₂ diphosphate H H H H NH-acetyl diphosphate H H H H NH-cyclopropyl diphosphate H H H H NH-methyl diphosphate H H H H NH-ethyl diphosphate H H H H OH diphosphate H H H H O-acetyl diphosphate H H H H OMe diphosphate H H H H OEt diphosphate H H H H O-cyclopropyl diphosphate H H H H SH diphosphate H H H H SMe diphosphate H H H H SEt diphosphate H H H H S-cyclopropyl diphosphate H H H H F diphosphate H H H H Cl diphosphate H H H H Br diphosphate H H H H I triphosphate H H H H NH₂ triphosphate H H H H NH-acetyl triphosphate H H H H NH-cyclopropyl triphosphate H H H H NH-methyl triphosphate H H H H NH-ethyl triphosphate H H H H OH triphosphate H H H H OMe triphosphate H H H H OEt triphosphate H H H H O-cyclopropyl triphosphate H H H H O-acetyl triphosphate H H H H SH triphosphate H H H H SMe triphosphate H H H H SEt triphosphate H H H H S-cyclopropyl triphosphate H H H H F triphosphate H H H H Cl triphosphate H H H H Br triphosphate H H H H I monophosphate monophosphate monophosphate H H NH₂ monophosphate monophosphate monophosphate H H NH-cyclopropyl monophosphate monophosphate monophosphate H H OH monophosphate monophosphate monophosphate H H F monophosphate monophosphate monophosphate H H Cl diphosphate diphosphate diphosphate H H NH₂ diphosphate diphosphate diphosphate H H NH-cyclopropyl diphosphate diphosphate diphosphate H H OH diphosphate diphosphate diphosphate H H F diphosphate diphosphate diphosphate H H Cl triphosphate triphosphate triphosphate H H NH₂ triphosphate triphosphate triphosphate H H NH-cyclopropyl triphosphate triphosphate triphosphate H H OH triphosphate triphosphate triphosphate H H F triphosphate triphosphate triphosphate H H Cl H H H F H NH₂ H H H F H NH-cyclopropyl H H H F H OH H H H F H F H H H F H Cl H H H Cl H NH₂ H H H Cl H NH-cyclopropyl H H H Cl H OH H H H Cl H F H H H Cl H Cl H H H Br H NH₂ H H H Br H NH-cyclopropyl H H H Br H OH H H H Br H F H H H Br H Cl H H H NH₂ H NH₂ H H H NH₂ H NH-cyclopropyl H H H NH₂ H OH H H H NH₂ H F H H H NH₂ H Cl H H H SH H NH₂ H H H SH H NH-cyclopropyl H H H SH H OH H H H SH H F H H H SH H Cl acetyl H H H H NH₂ acetyl H H H H NH-cyclopropyl acetyl H H H H OH acetyl H H H H F acetyl H H H H Cl acetyl H H F H NH₂ acetyl H H F H NH-cyclopropyl acetyl H H F H OH acetyl H H F H F acetyl H H F H Cl H acetyl acetyl H H NH₂ H acetyl acetyl H H NH-cyclopropyl H acetyl acetyl H H OH H acetyl acetyl H H F H acetyl acetyl H H Cl acetyl acetyl acetyl H H NH₂ acetyl acetyl acetyl H H NH-cyclopropyl acetyl acetyl acetyl H H OH acetyl acetyl acetyl H H F acetyl acetyl acetyl H H Cl monophosphate acetyl acetyl H H NH₂ monophosphate acetyl acetyl H H NH-cyclopropyl monophosphate acetyl acetyl H H OH monophosphate acetyl acetyl H H F monophosphate acetyl acetyl H H Cl diphosphate acetyl acetyl H H NH₂ diphosphate acetyl acetyl H H NH-cyclopropyl diphosphate acetyl acetyl H H OH diphosphate acetyl acetyl H H F diphosphate acetyl acetyl H H Cl triphosphate acetyl acetyl H H NH₂ triphosphate acetyl acetyl H H NH-cyclopropyl triphosphate acetyl acetyl H H OH triphosphate acetyl acetyl H H F triphosphate acetyl acetyl H H Cl H H H H NH₂ H H H H H NH₂ NH₂ H H H H NH₂ NH-cyclopropyl H H H H NH₂ NH-methyl H H H H NH₂ NH-ethyl H H H H NH₂ NH-acetyl H H H H NH₂ OH H H H H NH₂ OMe H H H H NH₂ OEt H H H H NH₂ O-cyclopropyl H H H H NH₂ O-acetyl H H H H NH₂ SH H H H H NH₂ SMe H H H H NH₂ SEt H H H H NH₂ S-cyclopropyl H H H H NH₂ F H H H H NH₂ Cl H H H H NH₂ Br H H H H NH₂ I monophosphate H H H NH₂ NH₂ monophosphate H H H NH₂ NH-acetyl monophosphate H H H NH₂ NH-cyclopropyl monophosphate H H H NH₂ NH-methyl monophosphate H H H NH₂ NH-ethyl monophosphate H H H NH₂ OH monophosphate H H H NH₂ O-acetyl monophosphate H H H NH₂ OMe monophosphate H H H NH₂ OEt monophosphate H H H NH₂ O-cyclopropyl monophosphate H H H NH₂ SH monophosphate H H H NH₂ SMe monophosphate H H H NH₂ SEt monophosphate H H H NH₂ S-cyclopropyl monophosphate H H H NH₂ F monophosphate H H H NH₂ Cl monophosphate H H H NH₂ Br monophosphate H H H NH₂ I diphosphate H H H NH₂ NH₂ diphosphate H H H NH₂ NH-acetyl diphosphate H H H NH₂ NH-cyclopropyl diphosphate H H H NH₂ NH-methyl diphosphate H H H NH₂ NH-ethyl diphosphate H H H NH₂ OH diphosphate H H H NH₂ O-acetyl diphosphate H H H NH₂ OMe diphosphate H H H NH₂ OEt diphosphate H H H NH₂ O-cyclopropyl diphosphate H H H NH₂ SH diphosphate H H H NH₂ SMe diphosphate H H H NH₂ SEt diphosphate H H H NH₂ S-cyclopropyl diphosphate H H H NH₂ F diphosphate H H H NH₂ Cl diphosphate H H H NH₂ Br diphosphate H H H NH₂ I triphosphate H H H NH₂ NH₂ triphosphate H H H NH₂ NH-acetyl triphosphate H H H NH₂ NH-cyclopropyl triphosphate H H H NH₂ NH-methyl triphosphate H H H NH₂ NH-ethyl triphosphate H H H NH₂ OH triphosphate H H H NH₂ OMe triphosphate H H H NH₂ OEt triphosphate H H H NH₂ O-cyclopropyl triphosphate H H H NH₂ O-acetyl triphosphate H H H NH₂ SH triphosphate H H H NH₂ SMe triphosphate H H H NH₂ SEt triphosphate H H H NH₂ S-cyclopropyl triphosphate H H H NH₂ F triphosphate H H H NH₂ Cl triphosphate H H H NH₂ Br triphosphate H H H NH₂ I monophosphate monophosphate monophosphate H NH₂ NH₂ monophosphate monophosphate monophosphate H NH₂ NH-cyclopropyl monophosphate monophosphate monophosphate H NH₂ OH monophosphate monophosphate monophosphate H NH₂ F monophosphate monophosphate monophosphate H NH₂ Cl diphosphate diphosphate diphosphate H NH₂ NH₂ diphosphate diphosphate diphosphate H NH₂ NH-cyclopropyl diphosphate diphosphate diphosphate H NH₂ OH diphosphate diphosphate diphosphate H NH₂ F diphosphate diphosphate diphosphate H NH₂ Cl triphosphate triphosphate triphosphate H NH₂ NH₂ triphosphate triphosphate triphosphate H NH₂ NH-cyclopropyl triphosphate triphosphate triphosphate H NH₂ OH triphosphate triphosphate triphosphate H NH₂ F triphosphate triphosphate triphosphate H NH₂ Cl H H H F NH₂ NH₂ H H H F NH₂ NH-cyclopropyl H H H F NH₂ OH H H H F NH₂ F H H H F NH₂ Cl H H H Cl NH₂ NH₂ H H H Cl NH₂ NH-cyclopropyl H H H Cl NH₂ OH H H H Cl NH₂ F H H H Cl NH₂ Cl H H H Br NH₂ NH₂ H H H Br NH₂ NH-cyclopropyl H H H Br NH₂ OH H H H Br NH₂ F H H H Br NH₂ Cl H H H NH₂ NH₂ NH₂ H H H NH₂ NH₂ NH-cyclopropyl H H H NH₂ NH₂ OH H H H NH₂ NH₂ F H H H NH₂ NH₂ Cl H H H SH NH₂ NH₂ H H H SH NH₂ NH-cyclopropyl H H H SH NH₂ OH H H H SH NH₂ F H H H SH NH₂ Cl acetyl H H H NH₂ NH₂ acetyl H H H NH₂ NH-cyclopropyl acetyl H H H NH₂ OH acetyl H H H NH₂ F acetyl H H H NH₂ Cl acetyl H H F NH₂ NH₂ acetyl H H F NH₂ NH-cyclopropyl acetyl H H F NH₂ OH acetyl H H F NH₂ F acetyl H H F NH₂ Cl H acetyl acetyl H NH₂ NH₂ H acetyl acetyl H NH₂ NH-cyclopropyl H acetyl acetyl H NH₂ OH H acetyl acetyl H NH₂ F H acetyl acetyl H NH₂ Cl acetyl acetyl acetyl H NH₂ NH₂ acetyl acetyl acetyl H NH₂ NH-cyclopropyl acetyl acetyl acetyl H NH₂ OH acetyl acetyl acetyl H NH₂ F acetyl acetyl acetyl H NH₂ Cl monophosphate acetyl acetyl H NH₂ NH₂ monophosphate acetyl acetyl H NH₂ NH-cyclopropyl monophosphate acetyl acetyl H NH₂ OH monophosphate acetyl acetyl H NH₂ F monophosphate acetyl acetyl H NH₂ Cl diphosphate acetyl acetyl H NH₂ NH₂ diphosphate acetyl acetyl H NH₂ NH-cyclopropyl diphosphate acetyl acetyl H NH₂ OH diphosphate acetyl acetyl H NH₂ F diphosphate acetyl acetyl H NH₂ Cl triphosphate acetyl acetyl H NH₂ NH₂ triphosphate acetyl acetyl H NH₂ NH-cyclopropyl triphosphate acetyl acetyl H NH₂ OH triphosphate acetyl acetyl H NH₂ F triphosphate acetyl acetyl H NH₂ Cl H H H H Cl H H H H H Cl H H H H H Cl NH₂ H H H H Cl NH-cyclopropyl H H H H Cl NH-methyl H H H H Cl NH-ethyl H H H H Cl NH-acetyl H H H H Cl OH H H H H Cl OMe H H H H Cl OEt H H H H Cl O-cyclopropyl H H H H Cl O-acetyl H H H H Cl SH H H H H Cl SMe H H H H Cl SEt H H H H Cl S-cyclopropyl monophosphate H H H Cl NH₂ monophosphate H H H Cl NH-acetyl monophosphate H H H Cl NH-cyclopropyl monophosphate H H H Cl NH-methyl monophosphate H H H Cl NH-ethyl monophosphate H H H Cl OH monophosphate H H H Cl O-acetyl monophosphate H H H Cl OMe monophosphate H H H Cl OEt monophosphate H H H Cl O-cyclopropyl monophosphate H H H Cl SH monophosphate H H H Cl SMe monophosphate H H H Cl SEt monophosphate H H H Cl S-cyclopropyl diphosphate H H H Cl NH₂ diphosphate H H H Cl NH-acetyl diphosphate H H H Cl NH-cyclopropyl diphosphate H H H Cl NH-methyl diphosphate H H H Cl NH-ethyl diphosphate H H H Cl OH diphosphate H H H Cl O-acetyl diphosphate H H H Cl OMe diphosphate H H H Cl OEt diphosphate H H H Cl O-cyclopropyl diphosphate H H H Cl SH diphosphate H H H Cl SMe diphosphate H H H Cl SEt diphosphate H H H Cl S-cyclopropyl triphosphate H H H Cl NH₂ triphosphate H H H Cl NH-acetyl triphosphate H H H Cl NH-cyclopropyl triphosphate H H H Cl NH-methyl triphosphate H H H Cl NH-ethyl triphosphate H H H Cl OH triphosphate H H H Cl OMe triphosphate H H H Cl OEt triphosphate H H H Cl O-cyclopropyl triphosphate H H H Cl O-acetyl triphosphate H H H Cl SH triphosphate H H H Cl SMe triphosphate H H H Cl SEt triphosphate H H H Cl S-cyclopropyl monophosphate monophosphate monophosphate H Cl NH₂ monophosphate monophosphate monophosphate H Cl NH-cyclopropyl monophosphate monophosphate monophosphate H Cl OH diphosphate diphosphate diphosphate H Cl NH₂ diphosphate diphosphate diphosphate H Cl NH-cyclopropyl diphosphate diphosphate diphosphate H Cl OH triphosphate triphosphate triphosphate H Cl NH₂ triphosphate triphosphate triphosphate H Cl NH-cyclopropyl triphosphate triphosphate triphosphate H Cl OH H H H F Cl NH₂ H H H F Cl NH-cyclopropyl H H H F Cl OH H H H Cl Cl NH₂ H H H Cl Cl NH-cyclopropyl H H H Cl Cl OH H H H Br Cl NH₂ H H H Br Cl NH-cyclopropyl H H H Br Cl OH H H H NH₂ Cl NH₂ H H H NH₂ Cl NH-cyclopropyl H H H NH₂ Cl OH H H H SH Cl NH₂ H H H SH Cl NH-cyclopropyl H H H SH Cl OH acetyl H H H Cl NH₂ acetyl H H H Cl NH-cyclopropyl acetyl H H H Cl OH acetyl H H F Cl NH₂ acetyl H H F Cl NH-cyclopropyl acetyl H H F Cl OH H acetyl acetyl H Cl NH₂ H acetyl acetyl H Cl NH-cyclopropyl H acetyl acetyl H Cl OH acetyl acetyl acetyl H Cl NH₂ acetyl acetyl acetyl H Cl NH-cyclopropyl acetyl acetyl acetyl H Cl OH monophosphate acetyl acetyl H Cl NH₂ monophosphate acetyl acetyl H Cl NH-cyclopropyl monophosphate acetyl acetyl H Cl OH diphosphate acetyl acetyl H Cl NH₂ diphosphate acetyl acetyl H Cl NH-cyclopropyl diphosphate acetyl acetyl H Cl OH triphosphate acetyl acetyl H Cl NH₂ triphosphate acetyl acetyl H Cl NH-cyclopropyl triphosphate acetyl acetyl H Cl OH H H H H Cl NH₂ H H H H Cl NH-cyclopropyl H H H H Cl OH H H H H Br NH₂ H H H H Br NH-cyclopropyl H H H H Br OH

Alternatively, the following nucleosides of Formula VI are prepared, using the appropriate sugar and pyrimidine or purine bases.

(VI)

wherein: R¹ R² R³ X¹ Y H H H H H H H H H NH₂ H H H H NH-cyclopropyl H H H H NH-methyl H H H H NH-ethyl H H H H NH-acetyl H H H H OH H H H H OMe H H H H OEt H H H H O-cyclopropyl H H H H O-acetyl H H H H SH H H H H SMe H H H H SEt H H H H S-cyclopropyl monophosphate H H H NH₂ monophosphate H H H NH-acetyl monophosphate H H H NH-cyclopropyl monophosphate H H H NH-methyl monophosphate H H H NH-ethyl monophosphate H H H OH monophosphate H H H O-acetyl monophosphate H H H OMe monophosphate H H H OEt monophosphate H H H O-cyclopropyl monophosphate H H H SH monophosphate H H H SMe monophosphate H H H SEt monophosphate H H H S-cyclopropyl diphosphate H H H NH₂ diphosphate H H H NH-acetyl diphosphate H H H NH-cyclopropyl diphosphate H H H NH-methyl diphosphate H H H NH-ethyl diphosphate H H H OH diphosphate H H H O-acetyl diphosphate H H H OMe diphosphate H H H OEt diphosphate H H H O-cyclopropyl diphosphate H H H SH diphosphate H H H SMe diphosphate H H H SEt diphosphate H H H S-cyclopropyl triphosphate H H H NH₂ triphosphate H H H NH-acetyl triphosphate H H H NH-cyclopropyl triphosphate H H H NH-methyl triphosphate H H H NH-ethyl triphosphate H H H OH triphosphate H H H OMe triphosphate H H H OEt triphosphate H H H O-cyclopropyl triphosphate H H H O-acetyl triphosphate H H H SH triphosphate H H H SMe triphosphate H H H SEt triphosphate H H H S-cyclopropyl monophosphate monophosphate monophosphate H NH₂ monophosphate monophosphate monophosphate H NH-cyclopropyl monophosphate monophosphate monophosphate H OH diphosphate diphosphate diphosphate H NH₂ diphosphate diphosphate diphosphate H NH-cyclopropyl diphosphate diphosphate diphosphate H OH triphosphate triphosphate triphosphate H NH₂ triphosphate triphosphate triphosphate H NH-cyclopropyl triphosphate triphosphate triphosphate H OH H H H F NH₂ H H H F NH-cyclopropyl H H H F OH H H H Cl NH₂ H H H Cl NH-cyclopropyl H H H Cl OH H H H Br NH₂ H H H Br NH-cyclopropyl H H H Br OH H H H NH₂ NH₂ H H H NH₂ NH-cyclopropyl H H H NH₂ OH H H H SH NH₂ H H H SH NH-cyclopropyl H H H SH OH acetyl H H H NH₂ acetyl H H H NH-cyclopropyl acetyl H H H OH acetyl H H F NH₂ acetyl H H F NH-cyclopropyl acetyl H H F OH H acetyl acetyl H NH₂ H acetyl acetyl H NH-cyclopropyl H acetyl acetyl H OH acetyl acetyl acetyl H NH₂ acetyl acetyl acetyl H NH-cyclopropyl acetyl acetyl acetyl H OH monophosphate acetyl acetyl H NH₂ monophosphate acetyl acetyl H NH-cyclopropyl monophosphate acetyl acetyl H OH diphosphate acetyl acetyl H NH₂ diphosphate acetyl acetyl H NH-cyclopropyl diphosphate acetyl acetyl H OH triphosphate acetyl acetyl H NH₂ triphosphate acetyl acetyl H NH-cyclopropyl triphosphate acetyl acetyl H OH

Alternatively, the following nucleosides of Formula XIII are prepared, using the appropriate sugar and pyrimidine or purine bases.

(XIII)

wherein: R¹ R² R³ R⁶ X Base H H H CH₃ O 2,4-O- Diacetyluracil H H H CH₃ O Hypoxanthine H H H CH₃ O 2,4-O- Diacetylthymine H H H CH₃ O Thymine H H H CH₃ O Cytosine H H H CH₃ O 4-(N-mono- acetyl)cytosine H H H CH₃ O 4-(N,N- diacetyl)cytosine H H H CH₃ O Uracil H H H CH₃ O 5-Fluorouracil H H H CH₃ S 2,4-O- Diacetyluraci H H H CH₃ S Hypoxanthine H H H CH₃ S 2,4-O- Diacetylthymine H H H CH₃ S Thymine H H H CH₃ S Cytosine H H H CH₃ S 4-(N-mono- acetyl)cytosine H H H CH₃ S 4-(N,N- diacetyl)cytosine H H H CH₃ S Uracil H H H CH₃ S 5-Fluorouracil monophosphate H H CH₃ O 2,4-O- Diacetyluracil monophosphate H H CH₃ O Hypoxanthine monophosphate H H CH₃ O 2,4-O- Diacetylthym monophosphate H H CH₃ O Thymine monophosphate H H CH₃ O Cytosine monophosphate H H CH₃ O 4-(N-mono- acetyl)cytosine monophosphate H H CH₃ O 4-(N,N- diacetyl)cytosine monophosphate H H CH₃ O Uracil monophosphate H H CH₃ O 5-Fluorouracil monophosphate H H CH₃ S 2,4-O- Diacetyluracil monophosphate H H CH₃ S Hypoxanthine monophosphate H H CH₃ S 2,4-O- Diacetylthym monophosphate H H CH₃ S Thymine monophosphate H H CH₃ S Cytosine monophosphate H H CH₃ S 4-(N-mono- acetyl)cytosine monophosphate H H CH₃ S 4-(N,N- diacetyl)cytosine monophosphate H H CH₃ S Uracil monophosphate H H CH₃ S 5-Fluorouracil diphosphate H H CH₃ O 2,4-O- Diacetyluracil diphosphate H H CH₃ O Hypoxanthine diphosphate H H CH₃ O 2,4-O- Diacetylthymine diphosphate H H CH₃ O Thymine diphosphate H H CH₃ O Cytosine diphosphate H H CH₃ O 4-(N-mono- acetyl)cytosine diphosphate H H CH₃ O 4-(N,N- diacetyl)cytosine diphosphate H H CH₃ O Uracil diphosphate H H CH₃ O 5-Fluorouracil diphosphate H H CH₃ S 2,4-O- Diacetyluracil diphosphate H H CH₃ S Hypoxanthine diphosphate H H CH₃ S 2,4-O- Diacetylthym diphosphate H H CH₃ S Thymine diphosphate H H CH₃ S Cytosine triphosphate H H CH₃ O 2,4-O- Diacetyluracil triphosphate H H CH₃ O Hypoxanthine triphosphate H H CH₃ O 2,4-O- Diacetylthymine triphosphate H H CH₃ O Thymine triphosphate H H CH₃ O Cytosine triphosphate H H CH₃ O 4-(N-mono- acetyl)cytosine triphosphate H H CH₃ O 4-(N,N- diacetyl)cytosine triphosphate H H CH₃ O Uracil triphosphate H H CH₃ O 5-Fluorouracil triphosphate H H CH₃ S 2,4-O- Diacetyluracil triphosphate H H CH₃ S Hypoxanthine triphosphate H H CH₃ S 2,4-O- Diacetylthymine triphosphate H H CH₃ S Thymine triphosphate H H CH₃ S Cytosine monophosphate mono- mono- CF₃ O 2,4-O- phosphate phosphate Diacetyluracil monophosphate mono- mono- CF₃ O Hypoxanthine phosphate phosphate monophosphate mono- mono- CF₃ O 2,4-O- phosphate phosphate Diacetylthymine monophosphate mono- mono- CF₃ O Thymine phosphate phosphate monophosphate mono- mono- CF₃ O Cytosine phosphate phosphate monophosphate mono- mono- CF₃ O 4-(N-mono- phosphate phosphate acetyl)cytosine monophosphate mono- mono- CF₃ O 4-(N,N- phosphate phosphate diacetyl)cytosine monophosphate mono- mono- CF₃ O Uracil phosphate phosphate monophosphate mono- mono- CF₃ O 5-Fluorouracil phosphate phosphate monophosphate mono- mono- CF₃ S 2,4-O- phosphate phosphate Diacetyluracil monophosphate mono- mono- CF₃ S Hypoxanthine phosphate phosphate monophosphate mono- mono- CF₃ S 2,4-O- phosphate phosphate Diacetylthymine monophosphate mono- mono- CF₃ S Thymine phosphate phosphate monophosphate mono- mono- CF₃ S Cytosine phosphate phosphate monophosphate mono- mono- CF₃ S 4-(N-mono- phosphate phosphate acetyl)cytosine monophosphate mono- mono- CF₃ S 4-(N,N- phosphate phosphate diacetyl)cytosine monophosphate mono- mono- CF₃ S Uracil phosphate phosphate monophosphate mono- mono- CF₃ S 5-Fluorouracil phosphate phosphate acetyl acetyl acetyl CF₃ O 4-(N,N- diacetyl)cytosine acetyl acetyl acetyl CF₃ S 4-(N,N- diacetyl)cytosine acetyl acetyl acetyl 2-bromo- O 4-(N,N- vinyl diacetyl)cytosine acetyl acetyl acetyl 2-bromo- S 4-(N,N- vinyl diacetyl)cytosine H H H CH₃ O 2-(N,N- diacetyl)- guanine H H H CH₃ O 6-O-acetyl guanine H H H CH₃ O 8-fluoroguanine H H H CH₃ O guanine H H H CH₃ O 6-(N,N- diacetyl)- adenine H H H CH₃ O 2-fluoroadenine H H H CH₃ O 8-fluoroadenine H H H CH₃ O 2,8-difluoro- adenine H H H CH₃ O adenine H H H CH₃ S 2-(N,N- diacetyl)- guanine H H H CH₃ S 6-O-acetyl guanine H H H CH₃ S 8-fluoroguanine H H H CH₃ S guanine H H H CH₃ S 6-(N,N- diacetyl)- adenine H H H CH₃ S 2-fluoroadenine H H H CH₃ S 8-fluoroadenine H H H CH₃ S 2,8-difluoro- adenine H H H CH₃ S adenine monophosphate H H CH₃ O 2-(N,N- diacetyl)- guanine monophosphate H H CH₃ O 6-O-acetyl guanine monophosphate H H CH₃ O 8-fluoroguanine monophosphate H H CH₃ O guanine monophosphate H H CH₃ O 6-(N,N- diacetyl)- adenine monophosphate H H CH₃ O 2-fluoroadenine monophosphate H H CH₃ O 8-fluoroadenine monophosphate H H CH₃ O 2,8-difluoro- adenine monophosphate H H CH₃ O adenine monophosphate H H CH₃ S 2-(N,N- diacetyl)- guanine monophosphate H H CH₃ S 6-O-acetyl guanine monophosphate H H CH₃ S 8-fluoroguanine monophosphate H H CH₃ S guanine monophosphate H H CH₃ S 6-(N,N- diacetyl)- adenine monophosphate H H CH₃ S 2-fluoroadenine monophosphate H H CH₃ S 8-fluoroadenine monophosphate H H CH₃ S 2,8-difluoro- adenine monophosphate H H CH₃ S adenine diphosphate H H CH₃ O 2-(N,N- diacetyl)- guanine diphosphate H H CH₃ O 6-O-acetyl guanine diphosphate H H CH₃ O 8-fluoroguanine diphosphate H H CH₃ O guanine diphosphate H H CH₃ O 6-(N,N- diacetyl)- adenine diphosphate H H CH₃ O 2-fluoroadenine diphosphate H H CH₃ O 8-fluoroadenine diphosphate H H CH₃ O 2,8-difluoro- adenine diphosphate H H CH₃ O adenine diphosphate H H CH₃ S 2-(N,N- diacetyl)- guanine diphosphate H H CH₃ S 6-O-acetyl guanine diphosphate H H CH₃ S 8-fluoroguanine diphosphate H H CH₃ S guanine diphosphate H H CH₃ S 6-(N,N- diacetyl)- adenine diphosphate H H CH₃ S 2-fluoroadenine diphosphate H H CH₃ S 8-fluoroadenine diphosphate H H CH₃ S 2,8-difluoro- adenine diphosphate H H CH₃ S adenine triphosphate H H CH₃ O 2-(N,N- diacetyl)- guanine triphosphate H H CH₃ O 6-O-acetyl guanine triphosphate H H CH₃ O 8-fluoroguanine triphosphate H H CH₃ O guanine triphosphate H H CH₃ O 6-(N,N- diacetyl)- adenine triphosphate H H CH₃ O 2-fluoroadenine triphosphate H H CH₃ O 8-fluoroadenine triphosphate H H CH₃ O 2,8-difluoro- adenine triphosphate H H CH₃ O 2-(N,N- diacetyl)- guanine triphosphate H H CH₃ S 6-O-acetyl guanine triphosphate H H CH₃ S 8-fluoroguanine triphosphate H H CH₃ S guanine triphosphate H H CH₃ S 6-(N,N- diacetyl)- adenine triphosphate H H CH₃ S 2-fluoroadenine triphosphate H H CH₃ S 8-fluoroadenine triphosphate H H CH₃ S 2,8-difluoro- adenine triphosphate H H CH₃ S adenine monophosphate mono- mono- CF₃ O 2-(N,N- phosphate phosphate diacetyl)- guanine monophosphate mono- mono- CF₃ O 6-O-acetyl phosphate phosphate guanine monophosphate mono- mono- CF₃ O 8-fluoroguanine phosphate phosphate monophosphate mono- mono- CF₃ O guanine phosphate phosphate monophosphate mono- mono- CF₃ O 6-(N,N- phosphate phosphate diacetyl)- adenine monophosphate mono- mono- CF₃ O 2-fluoroadenine phosphate phosphate monophosphate mono- mono- CF₃ O 8-fluoroadenine phosphate phosphate monophosphate mono- mono- CF₃ O 2,8-difluoro- phosphate phosphate adenine monophosphate mono- mono- CF₃ O adenine phosphate phosphate monophosphate mono- mono- CF₃ S 2-(N,N- phosphate phosphate diacetyl)- guanine monophosphate mono- mono- CF₃ S 6-O-acetyl phosphate phosphate guanine monophosphate mono- mono- CF₃ S 8-fluoroguanine phosphate phosphate monophosphate mono- mono- CF₃ S guanine phosphate phosphate monophosphate mono- mono- CF₃ S 6-(N,N- phosphate phosphate diacetyl)- adenine monophosphate mono- mono- CF₃ S 2-fluoroadenine phosphate phosphate monophosphate mono- mono- CF₃ S 8-fluoroadenine phosphate phosphate monophosphate mono- mono- CF₃ S 2,8-difluoro- phosphate phosphate adenine monophosphate mono- mono- CF₃ S adenine phosphate phosphate acetyl acetyl acetyl CF₃ O guanine acetyl acetyl acetyl CF₃ S guanine acetyl acetyl acetyl 2-bromo- O guanine vinyl acetyl acetyl acetyl 2-bromo- S guanine vinyl

Alternatively, the following nucleosides of Formula XIV are prepared, using the appropriate sugar and pyrimidine or purine bases.

(XIV)

wherein: R¹ R² R⁶ X Base H H CH₃ O 2,4-O-Diacetyluracil H H CH₃ O Hypoxanthine H H CH₃ O 2,4-O-Diacetylthymine H H CH₃ O Thymine H H CH₃ O Cytosine H H CH₃ O 4-(N-mono-acetyl)cytosine H H CH₃ O 4-(N,N-diacetyl)cytosine H H CH₃ O Uracil H H CH₃ O 5-Fluorouracil H H CH₃ S 2,4-O-Diacetyluracil H H CH₃ S Hypoxanthine H H CH₃ S 2,4-O-Diacetylthymine H H CH₃ S Thymine H H CH₃ S Cytosine H H CH₃ S 4-(N-mono-acetyl)cytosin H H CH₃ S 4-(N,N-diacetyl)cytosine H H CH₃ S Uracil H H CH₃ S 5-Fluorouracil monophosphate H CH₃ O 2,4-O-Diacetyluracil monophosphate H CH₃ O Hypoxanthine monophosphate H CH₃ O 2,4-O-Diacetylthym monophosphate H CH₃ O Thymine monophosphate H CH₃ O Cytosine monophosphate H CH₃ O 4-(N-mono-acetyl)cytosine monophosphate H CH₃ O 4-(N,N-diacetyl)cytos monophosphate H CH₃ O Uracil monophosphate H CH₃ O 5-Fluorouracil monophosphate H CH₃ S 2,4-O-Diacetyluracil monophosphate H CH₃ S Hypoxanthine monophosphate H CH₃ S 2,4-O-Diacetylthym monophosphate H CH₃ S Thymine monophosphate H CH₃ S Cytosine monophosphate H CH₃ S 4-(N-mono-acetyl)cytosine monophosphate H CH₃ S 4-(N,N-diacetyl)cytosine monophosphate H CH₃ S Uracil monophosphate H CH₃ S 5-Fluorouracil diphosphate H CH₃ O 2,4-O-Diacetyluracil diphosphate H CH₃ O Hypoxanthine diphosphate H CH₃ O 2,4-O-Diacetylthymine diphosphate H CH₃ O Thymine diphosphate H CH₃ O Cytosine diphosphate H CH₃ O 4-(N-mono-acetyl)cytosine diphosphate H CH₃ O 4-(N,N-diacetyl)cytosine diphosphate H CH₃ O Uracil diphosphate H CH₃ O 5-Fluorouracil diphosphate H CH₃ S 2,4-O-Diacetyluracil diphosphate H CH₃ S Hypoxanthine diphosphate H CH₃ S 2,4-O-Diacetylthymine diphosphate H CH₃ S Thymine diphosphate H CH₃ S Cytosine triphosphate H CH₃ O 2,4-O-Diacetyluracil triphosphate H CH₃ O Hypoxanthine triphosphate H CH₃ O 2,4-O-Diacetylthymine triphosphate H CH₃ O Thymine triphosphate H CH₃ O Cytosine triphosphate H CH₃ O 4-(N-mono-acetyl)cytosine triphosphate H CH₃ O 4-(N,N-diacetyl)cytosine triphosphate H CH₃ O Uracil triphosphate H CH₃ O 5-Fluorouracil triphosphate H CH₃ S 2,4-O-Diacetyluracil triphosphate H CH₃ S Hypoxanthine triphosphate H CH₃ S 2,4-O-Diacetylthymine triphosphate H CH₃ S Thymine triphosphate H CH₃ S Cytosine monophosphate monophosphate CF₃ O 2,4-O-Diacetyluracil monophosphate monophosphate CF₃ O Hypoxanthine monophosphate monophosphate CF₃ O 2,4-O-Diacetylthymine monophosphate monophosphate CF₃ O Thymine monophosphate monophosphate CF₃ O Cytosine monophosphate monophosphate CF₃ O 4-(N-mono-acetyl)cytosine monophosphate monophosphate CF₃ O 4-(N,N-diacetyl)cytosine monophosphate monophosphate CF₃ O Uracil monophosphate monophosphate CF₃ O 5-Fluorouracil monophosphate monophosphate CF₃ S 2,4-O-Diacetyluracil monophosphate monophosphate CF₃ S Hypoxanthine monophosphate monophosphate CF₃ S 2,4-O-Diacetylthymine monophosphate monophosphate CF₃ S Thymine monophosphate monophosphate CF₃ S Cytosine monophosphate monophosphate CF₃ S 4-(N-mono-acetyl)cytosine monophosphate monophosphate CF₃ S 4-(N,N-diacetyl)cytosine monophosphate monophosphate CF₃ S Uracil monophosphate monophosphate CF₃ S 5-Fluorouracil acetyl acetyl CF₃ O 4-(N,N-diacetyl)cytosine acetyl acetyl CF₃ S 4-(N,N-diacetyl)cytosine acetyl acetyl 2- O 4-(N,N-diacetyl)cytosine bromo- vinyl acetyl acetyl 2- S 4-(N,N-diacetyl)cytosine bromo- vinyl

Alternatively, the following nucleosides of Formula XV are prepared, using the appropriate sugar and pyrimidine or purine bases.

(XV)

wherein: R¹ R⁶ X Base H CH₃ O 2,4-O-Diacetyluracil H CH₃ O Hypoxanthine H CH₃ O 2,4-O-Diacetylthymine H CH₃ O Thymine H CH₃ O Cytosine H CH₃ O 4-(N-mono-acetyl)cytosine H CH₃ O 4-(N,N-diacetyl)cytosine H CH₃ O Uracil H CH₃ O 5-Fluorouracil H CH₃ S 2,4-O-Diacetyluracil H CH₃ S Hypoxanthine H CH₃ S 2,4-O-Diacetylthymine H CH₃ S Thymine H CH₃ S Cytosine H CH₃ S 4-(N-mono-acetyl)cytosine H CH₃ S 4-(N,N-diacetyl)cytosine H CH₃ S Uracil H CH₃ S 5-Fluorouracil monophosphate CH₃ O 2,4-O-Diacetyluracil monophosphate CH₃ O Hypoxanthine monophosphate CH₃ O 2,4-O-Diacetylthymine monophosphate CH₃ O Thymine monophosphate CH₃ O Cytosine monophosphate CH₃ O 4-(N-mono-acetyl)cytosine monophosphate CH₃ O 4-(N,N-diacetyl)cytosine monophosphate CH₃ O Uracil monophosphate CH₃ O 5-Fluorouracil monophosphate CH₃ S 2,4-O-Diacetyluracil monophosphate CH₃ S Hypoxanthine monophosphate CH₃ S 2,4-O-Diacetylthymine monophosphate CH₃ S Thymine monophosphate CH₃ S Cytosine monophosphate CH₃ S 4-(N-mono-acetyl)cytosine monophosphate CH₃ S 4-(N,N-diacetyl)cytosine monophosphate CH₃ S Uracil monophosphate CH₃ S 5-Fluorouracil diphosphate CH₃ O 2,4-O-Diacetyluracil diphosphate CH₃ O Hypoxanthine diphosphate CH₃ O 2,4-O-Diacetylthymine diphosphate CH₃ O Thymine diphosphate CH₃ O Cytosine diphosphate CH₃ O 4-(N-mono-acetyl)cytosine diphosphate CH₃ O 4-(N,N-diacetyl)cytosine diphosphate CH₃ O Uracil diphosphate CH₃ O 5-Fluorouracil diphosphate CH₃ S 2,4-O-Diacetyluracil diphosphate CH₃ S Hypoxanthine diphosphate CH₃ S 2,4-O-Diacetylthymine diphosphate CH₃ S Thymine diphosphate CH₃ S Cytosine triphosphate CH₃ O 2,4-O-Diacetyluracil triphosphate CH₃ O Hypoxanthine triphosphate CH₃ O 2,4-O-Diacetylthymine triphosphate CH₃ O Thymine triphosphate CH₃ O Cytosine triphosphate CH₃ O 4-(N-mono-acetyl)cytosine triphosphate CH₃ O 4-(N,N-diacetyl)cytosine triphosphate CH₃ O Uracil triphosphate CH₃ O 5-Fluorouracil triphosphate CH₃ S 2,4-O-Diacetyluracil triphosphate CH₃ S Hypoxanthine triphosphate CH₃ S 2,4-O-Diacetylthymine triphosphate CH₃ S Thymine triphosphate CH₃ S Cytosine monophosphate CF₃ O 2,4-O-Diacetyluracil monophosphate CF₃ O Hypoxanthine monophosphate CF₃ O 2,4-O-Diacetylthymine monophosphate CF₃ O Thymine monophosphate CF₃ O Cytosine monophosphate CF₃ O 4-(N-mono-acetyl)cytosine monophosphate CF₃ O 4-(N,N-diacetyl)cytosine monophosphate CF₃ O Uracil monophosphate CF₃ O 5-Fluorouracil monophosphate CF₃ S 2,4-O-Diacetyluracil monophosphate CF₃ S Hypoxanthine monophosphate CF₃ S 2,4-O-Diacetylthymine monophosphate CF₃ S Thymine monophosphate CF₃ S Cytosine monophosphate CF₃ S 4-(N-mono-acetyl)cytosine monophosphate CF₃ S 4-(N,N-diacetyl)cytosine monophosphate CF₃ S Uracil monophosphate CF₃ S 5-Fluorouracil acetyl CF₃ O 4-(N,N-diacetyl)cytosine acetyl CF₃ S 4-(N,N-diacetyl)cytosine acetyl 2-bromo-vinyl O 4-(N,N-diacetyl)cytosine acetyl 2-bromo-vinyl S 4-(N,N-diacetyl)cytosine

Alternatively, the following nucleosides of Formula XVIII are prepared, using the appropriate sugar and pyrimidine or purine bases.

(XVIII)

wherein: R¹ R⁶ R⁷ X Base R⁸ R⁹ H CH₃ OH O 2,4-O-Diacetyluracil H Me H CH₃ OH O Hypoxanthine H Me H CH₃ OH O 2,4-O-Diacetylthymine H Me H CH₃ OH O Thymine H Me H CH₃ OH O Cytosine H Me H CH₃ OH O 4-(N-mono-acetyl)cytosine H Me H CH₃ OH O 4-(N,N-diacetyl)cytosine H Me H CH₃ OH O Uracil H Me H CH₃ OH O 5-Fluorouracil H Me H CH₃ OH S 2,4-O-Diacetyluracil H Me H CH₃ OH S Hypoxanthine H Me H CH₃ OH S 2,4-O-Diacetylthymine H Me H CH₃ OH S Thymine H Me H CH₃ OH S Cytosine H Me H CH₃ OH S 4-(N-mono-acetyl)cytosine H Me H CH₃ OH S 4-(N,N-diacetyl)cytosine H Me H CH₃ OH S Uracil H Me H CH₃ OH S 5-Fluorouracil H Me monophosphate CH₃ OH O 2,4-O-Diacetyluracil H Me monophosphate CH₃ OH O Hypoxanthine H Me monophosphate CH₃ OH O 2,4-O-Diacetylthymine H Me monophosphate CH₃ OH O Thymine H Me monophosphate CH₃ OH O Cytosine H Me monophosphate CH₃ OH O 4-(N-mono-acetyl)cytosine H Me monophosphate CH₃ OH O 4-(N,N-diacetyl)cytosine H Me monophosphate CH₃ OH O Uracil H Me monophosphate CH₃ OH O 5-Fluorouracil H Me monophosphate CH₃ OH S 2,4-O-Diacetyluracil H Me monophosphate CH₃ OH S Hypoxanthine H Me monophosphate CH₃ OH S 2,4-O-Diacetylthymine H Me monophosphate CH₃ OH S Thymine H Me monophosphate CH₃ OH S Cytosine H Me monophosphate CH₃ OH S 4-(N-mono-acetyl)cytosine H Me monophosphate CH₃ OH S 4-(N,N-diacetyl)cytosine H Me monophosphate CH₃ OH S Uracil H Me monophosphate CH₃ OH S 5-Fluorouracil H Me diphosphate CH₃ OH O 2,4-O-Diacetyluracil H Me diphosphate CH₃ OH O Hypoxanthine H Me diphosphate CH₃ OH O 2,4-O-Diacetylthymine H Me diphosphate CH₃ OH O Thymine H Me diphosphate CH₃ OH O Cytosine H Me diphosphate CH₃ OH O 4-(N-mono-acetyl)cytosine H Me diphosphate CH₃ OH O 4-(N,N-diacetyl)cytosine H Me diphosphate CH₃ OH O Uracil H Me diphosphate CH₃ OH O 5-Fluorouracil H Me diphosphate CH₃ OH S 2,4-O-Diacetyluracil H Me diphosphate CH₃ OH S Hypoxanthine H Me diphosphate CH₃ OH S 2,4-O-Diacetylthymine H Me diphosphate CH₃ OH S Thymine H Me diphosphate CH₃ OH S Cytosine H Me triphosphate CH₃ OH O 2,4-O-Diacetyluracil H Me triphosphate CH₃ OH O Hypoxanthine H Me triphosphate CH₃ OH O 2,4-O-Diacetylthymine H Me triphosphate CH₃ OH O Thymine H Me triphosphate CH₃ OH O Cytosine H Me triphosphate CH₃ OH O 4-(N-mono-acetyl)cytosine H Me triphosphate CH₃ OH O 4-(N,N-diacetyl)cytosine H Me triphosphate CH₃ OH O Uracil H Me triphosphate CH₃ OH O 5-Fluorouracil H Me triphosphate CH₃ OH S 2,4-O-Diacetyluracil H Me triphosphate CH₃ OH S Hypoxanthine H Me triphosphate CH₃ OH S 2,4-O-Diacetylthymine H Me triphosphate CH₃ OH S Thymine H Me triphosphate CH₃ OH S Cytosine H Me monophosphate CF₃ OH O 2,4-O-Diacetyluracil H Me monophosphate CF₃ OH O Hypoxanthine H Me monophosphate CF₃ OH O 2,4-O-Diacetylthymine H Me monophosphate CF₃ OH O Thymine H Me monophosphate CF₃ OH O Cytosine H Me monophosphate CF₃ OH O 4-(N-mono-acetyl)cytosine H Me monophosphate CF₃ OH O 4-(N,N-diacetyl)cytosine H Me monophosphate CF₃ OH O Uracil H Me monophosphate CF₃ OH O 5-Fluorouracil H Me monophosphate CF₃ OH S 2,4-O-Diacetyluracil H Me monophosphate CF₃ OH S Hypoxanthine H Me monophosphate CF₃ OH S 2,4-O-Diacetylthymine H Me monophosphate CF₃ OH S Thymine H Me monophosphate CF₃ OH S Cytosine H Me monophosphate CF₃ OH S 4-(N-mono-acetyl)cytosine H Me monophosphate CF₃ OH S 4-(N,N-diacetyl)cytosine H Me monophosphate CF₃ OH S Uracil H Me monophosphate CF₃ OH S 5-Fluorouracil H Me acetyl CH₃ OH O 4-(N,N-diacetyl)cytosine H Br acetyl CH₃ OH S 4-(N,N-diacetyl)cytosine H Br

VII. Anti-Hepatitis C Activity

Compounds can exhibit anti-hepatitis C activity by inhibiting HCV polymerase, by inhibiting other enzymes needed in the replication cycle, or by other pathways. A number of assays have been published to assess these activities. A general method that assesses the gross increase of HCV virus in culture is disclosed in U.S. Pat. No. 5,738,985 to Miles et al. In vitro assays have been reported in Ferrari et al., Jnl. of Vir., 73:1649-1654, 1999; Ishii et al., Hepatology, 29:1227-1235, 1999; Lohmann et al., Jnl. of Bio. Chem., 274:10807-10815, 1999; and Yamashita et al, Jnl. of Bio. Chem., 273:15479-15486, 1998.

WO 97/12033, filed on Sep. 27, 1996, by Emory University, listing C. Hagedorn and A. Reinoldus as inventors, and which claims priority to U.S. Ser. No. 60/004,383, filed on September 1995, describes an HCV polymerase assay that can be used to evaluate the activity of the compounds described herein. Another HCV polymerase assay has been reported by Bartholomeusz, et al., Hepatitis C virus (HCV) RNA polymerase assay using cloned HCV non-structural proteins; Antiviral Therapy 1996:1(Supp 4) 18-24.

Screens that measure reductions in kinase activity from HCV drugs are disclosed in U.S. Pat. No. 6,030,785, to Katze et al., U.S. Pat. No. 6,010,848 to Delvecchio et al, and U.S. Pat. No. 5,759,795 to Jubin et al. Screens that measure the protease inhibiting activity of proposed HCV drugs are disclosed in U.S. Pat. No. 5,861,267 to Su et al, U.S. Pat. No. 5,739,002 to De Francesco et al, and U.S. Pat. No. 5,597,691 to Houghton et al.

Example 4 Phosphorylation Assay of Nucleoside to Active Triphosphate

To determine the cellular metabolism of the compounds, HepG2 cells were obtained from the American Type Culture Collection (Rockville, Md.), and were grown in 225 cm² tissue culture flasks in minimal essential medium supplemented with non-essential amino acids, 1% penicillin-streptomycin. The medium was renewed every three days, and the cells were subcultured once a week. After detachment of the adherent monolayer with a 10 minute exposure to 30 mL of trypsin-EDTA and three consecutive washes with medium, confluent HepG2 cells were seeded at a density of 2.5×10⁶ cells per well in a 6-well plate and exposed to 10 μM of [³H] labeled active compound (500 dpm/μmol) for the specified time periods. The cells were maintained at 37° C. under a 5% CO₂ atmosphere. At the selected time points, the cells were washed three times with ice-cold phosphate-buffered saline (PBS). Intracellular active compound and its respective metabolites were extracted by incubating the cell pellet overnight at −20° C. with 60% methanol followed by extraction with an additional 20 μL of cold methanol for one hour in an ice bath. The extracts were then combined, dried under gentle filtered air flow and stored at −20° C. until HPLC analysis. The preliminary results of the HPLC analysis are tabulated in Table 1.

TABLE 1 [pmol/million cells] β-D-2′-CH₃- β-D-2′-CH₃- β-D-2′-CH₃- β-D-2′-CH₃- Time (h) riboA-TP riboU-TP riboC-TP riboG-TP 2 33.1 0.40 2.24 ND 4 67.7 1.21 3.99 ND 8 147 1.57 9.76 2.85 24 427 6.39 34.9 0.91 30 456 7.18 36.2 3.22 48 288 9.42 56.4 6.26

Example 5 Bioavailability Assay in Cynomolgus Monkeys

Within 1 week prior to the study initiation, the cynomolgus monkey was surgically implanted with a chronic venous catheter and subcutaneous venous access port (VAP) to facilitate blood collection and underwent a physical examination including hematology and serum chemistry evaluations and the body weight was recorded. Each monkey (six total), received approximately 250 uCi of ³H activity with each dose of active compound, namely β-D-2′-CH₃-riboG at a dose level of 10 mg/kg at a dose concentration of 5 mg/mL, either via an intravenous bolus (3 monkeys, IV), or via oral gavage (3 monkeys, PO). Each dosing syringe was weighed before dosing to gravimetrically determine the quantity of formulation administered. Urine samples were collected via pan catch at the designated intervals (approximately 18-0 hours pre-dose, 0-4, 4-8 and 8-12 hours post-dosage) and processed. Blood samples were collected as well (pre-dose, 0.25, 0.5, 1, 2, 3, 6, 8, 12 and 24 hours post-dosage) via the chronic venous catheter and VAP or from a peripheral vessel if the chronic venous catheter procedure should not be possible. The blood and urine samples were analyzed for the maximum concentration (C_(max)), time when the maximum concentration was achieved (T_(max)), area under the curve (AUC), half life of the dosage concentration (T_(1/2)), clearance (CL), steady state volume and distribution (V_(ss)) and bioavailability (F), which are tabulated in Tables 2 and 3, and graphically illustrated in FIGS. 2 and 3, respectively.

TABLE 2 Oral Bioavailability in Monkeys AUC Norm AUC Mean Norm Dose (ng/ (ng/mL × AUC (ng/ (mg) mL × h) h/mg) mL × h/mg) F (%) IV Monkey 1 46.44 13614 293.2 IV Monkey 2 24.53 6581 268.3 IV Monkey 3 20.72 6079 293.4 284.9 PO Monkey 1 29.04 758 26.1 PO Monkey 2 30.93 898 29.0 PO Monkey 3 30.04 1842 61.3 38.8 13.6

TABLE 3 Experimental Pharmacokinetics of β-D- 2′-CH₃-riboG in Cynomolgus Monkeys IV PO Dose/Route (mg/kg) 10 10 C_(max) (ng/mL) 6945.6 ± 1886.0  217.7 ± 132.1 T_(max) (hr) 0.25 ± 0.00  2.00 ± 1.00 AUC (ng/mL × hr) 8758.0 ± 4212.9 1166.0 ± 589.6 T_(1/2) (hr) 7.9 ± 5.4 10.3 ± 4.1 CL (L/hr/kg) 1.28 ± 0.48 V_(ss) (L/kg) 2.09 ± 0.54 F (%) 13.8

Example 6 Bone Marrow Toxicity Assay

Human bone marrow cells were collected from normal healthy volunteers and the mononuclear population was separated by Ficoll-Hypaque gradient centrifugation as described previously by Sommadossi J-P, Carlisle R. “Toxicity of 3′-azido-3′-deoxythymidine and 9-(1,3-dihydroxy-2-propoxymethyl)guanine for normal human hematopoietic progenitor cells in vitro” Antimicrobial Agents and Chemotherapy 1987; 31:452-454; and Sommadossi J-P, Schinazi R F, Chu CK, Xie M-Y. “Comparison of cytotoxicity of the (−)- and (+)-enantiomer of 2′,3′-dideoxy-3′-thiacytidine in normal human bone marrow progenitor cells” Biochemical Pharmacology 1992; 44:1921-1925. The culture assays for CFU-GM and BFU-E were performed using a bilayer soft agar or methylcellulose method. Drugs were diluted in tissue culture medium and filtered. After 14 to 18 days at 37° C. in a humidified atmosphere of 5% CO₂ in air, colonies of greater than 50 cells were counted using an inverted microscope. The results in Table 4 are presented as the percent inhibition of colony formation in the presence of drug compared to solvent control cultures.

TABLE 4 Human Bone Marrow Toxicity CFU-GM and BFU-E Clonogenic Assays IC₅₀ in μM Treatment CFU-GM BFU-E ribavirin ~5 ~1 β-D-2′-CH₃-riboA >100 >100 β-D-2′-CH₃-riboU >100 >100 β-D-2′-CH₃-riboC >10 >10 β-D-2′-CH₃-riboG >10 >100

Example 7 Mitochondria Toxicity Assay

HepG2 cells were cultured in 12-well plates as described above and exposed to various concentrations of drugs as taught by Pan-Zhou X-R, Cui L, Zhou X-J, Sommadossi J-P, Darley-Usmer VM. “Differential effects of antiretroviral nucleoside analogs on mitochondrial function in HepG2 cells” Antimicrob Agents Chemother 2000; 44:496-503. Lactic acid levels in the culture medium after 4 day drug exposure was measured using a Boehringer lactic acid assay kit. Lactic acid levels were normalized by cell number as measured by hemocytometer count. The preliminary results from this assay are tabulated in Table 5.

TABLE 5 Mitochondrial Toxicity Study (L-lactic acid assay) Conc. (μM) lactate (mg/10⁶ cell) % of Control Control 2.18 FIAU 10 3.73 170.4 β-D-2′-CH₃-riboC 1 2.52 115.3 10 2.36 107.9 50 2.26 103.4 100 2.21 101.2

This invention has been described with reference to its preferred embodiments. Variations and modifications of the invention, will be obvious to those skilled in the art from the foregoing detailed description of the invention. 

What is claimed is:
 1. A method for the treatment of a hepatitis C virus infection in a host, comprising administering to the host an anti-virally effective amount of a compound of Formula XVII:

or a pharmaceutically acceptable salt or ester thereof; wherein: Base is a pyrimidine base; R¹ and R² are each independently H, phosphate, monophosphate, diphosphate, triphosphoate, a stabilized phosphate prodrug, acyl, lower acyl, alkyl, lower alkyl, or a pharmaceutically acceptable leaving group which, when administered in vivo, provides a compound wherein R¹ and R² are each independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl, lower alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), halo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; R⁷ and R⁹ are each independently hydrogen, OR², hydroxy, alkyl, lower alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; R¹⁰ is H, alkyl, lower alkyl, or halo; alternatively, R⁷ and R⁹, or R⁷ and R¹⁰ can come together to form a bond; and X is O, S, SO₂, or CH₂.
 2. The method of claim 1, wherein R¹ and R² are each independently H; phosphate; a stabilized phosphate prodrug; acyl; or a pharmaceutically acceptable leaving group which, when administered in vivo, provides a compound wherein R¹ and R² are each independently H or phosphate.
 3. The method of claim 1, wherein R¹ is hydrogen, acyl, or phosphate.
 4. The method of claim 1, wherein R¹ is hydrogen or phosphate.
 5. The method of claim 1, wherein R¹ is phosphate.
 6. The method of claim 1, wherein R² is hydrogen or acyl.
 7. The method of claim 1, wherein R² is hydrogen.
 8. The method of claim 1, wherein R⁶ is alkyl.
 9. The method of claim 1, wherein R⁶ is methyl.
 10. The method of claim 1, wherein R⁷ and R⁹ are each independently hydrogen, OR², hydroxy, alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂.
 11. The method of claim 1, wherein R⁷ and R⁹ are each independently hydrogen, OR², alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —O(alkenyl), chloro, bromo, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂.
 12. The method of claim 1, wherein R⁷ and R⁹ are each independently hydrogen, OR², hydroxy, azido, cyano, alkynyl, chloro, bromo, iodo, or NH₂.
 13. The method of claim 1, wherein R⁷ is hydroxy.
 14. The method of claim 1, wherein R⁷ is azido.
 15. The method of claim 1, wherein R⁷ is cyano.
 16. The method of claim 1, wherein R⁷ is alkynyl.
 17. The method of claim 16, wherein R⁷ is ethynyl.
 18. The method of claim 1, wherein R⁷ is halo.
 19. The method of claim 1, wherein R⁷ is chloro, bromo, or iodo.
 20. The method of claim 1, wherein R⁷ is chloro.
 21. The method of claim 1, wherein R⁷ is NH₂.
 22. The method of claim 1, wherein R⁹ is hydroxy.
 23. The method of claim 1, wherein R⁷ and R⁹ are hydroxy.
 24. The method of claim 1, wherein R¹⁰ is H, alkyl, chloro, bromo, or iodo.
 25. The method of claim 1, wherein R¹⁰ is hydrogen.
 26. The method of claim 1, wherein X is O.
 27. The method of claim 1, wherein Base is selected from the group consisting of cytosinyl, 5-azacytocinyl, 6-azacytosinyl, 5-fluorocytosinyl, 5-methylcytosinyl, 6-azapyrimidinyl, 2-mercaptopyrmidinyl, 4-mercaptopyrmidinyl, C⁵-alkylpyrimidinyls, C⁵-benzylpyrimidinyls, C⁵-halopyrimidinyls, C⁵-vinylpyrimidinyl, C⁵-acetylenic pyrimidinyl, C⁵-acyl pyrimidinyl, C⁵-amidopyrimidinyl, C⁵-cyanopyrimidinyl, C⁵-nitropyrimidinyl, C⁵-aminopyrimidinyl, thyminyl, uracilyl, 5-halouracilyl, 5-fluorouracilyl, and 5-azauracilyl.
 28. The method of claim 1, wherein Base is cytosinyl, N-acetylcytosinyl, N,N-diacetyl)cytosinyl, N-methylcytosinyl, N-ethylcytosinyl, N-cyclopropylcytosinyl, thyminyl, 2,4-O-diacetylthyminyl, uracilyl, 5-fluorouracilyl, 4-O-acetyluracilyl, 2,4-O-diacetyluracilyl, 4-O-methyluracilyl, 4-O-ethyluracilyl, or 4-O-cyclopropyluracilyl.
 29. The method of claim 1, wherein Base is cytosinyl, thyminyl, or uracilyl.
 30. The method of claim 1, wherein Base is cytosinyl.
 31. The method of claim 1, wherein Base is thyminyl.
 32. The method of claim 1, wherein Base is uracilyl.
 33. The method of claim 1, wherein Base is selected from the group consisting of:


34. The method of claim 1, wherein Base is selected from the group consisting of:


35. The method of claim 1, wherein: Base is a pyrimidine base; R¹ and R² are each independently H; phosphate; a stabilized phosphate prodrug; acyl; or a pharmaceutically acceptable leaving group which, when administered in vivo, provides a compound wherein R¹ and R² are each independently H or phosphate; R⁶ is alkyl; R⁷ and R⁹ are each independently hydrogen, OR², hydroxy, alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; R¹⁰ is H, alkyl, chloro, bromo, or iodo; alternatively, R⁷ and R⁹, or R⁷ and R¹⁰ can come together to form a bond; and X is O.
 36. The method of claim 1, wherein: Base is a pyrimidine base; R¹ is hydrogen or phosphate; R² is hydrogen or acyl; R⁶ is alkyl; R⁷ and R⁹ are each independently hydrogen, OR², hydroxy, azido, cyano, alkynyl, chloro, bromo, or iodo; R¹⁰ is hydrogen; and X is O.
 37. A method for the treatment of a hepatitis C virus infection in a host, comprising administering to the host an anti-virally effective amount of a compound of Formula X or XI:

or a pharmaceutically acceptable salt or ester thereof; wherein: Base is a pyrimidine base; R¹, R², and R³ are each independently H, phosphate, monophosphate, diphosphate, triphosphoate, a stabilized phosphate prodrug, acyl, lower acyl, alkyl, lower alkyl, or a pharmaceutically acceptable leaving group which, when administered in vivo, provides a compound wherein R¹, R², and R³ are each independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl, lower alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), halo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; R⁷ is hydrogen, OR³, hydroxy, alkyl, lower alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), halo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; X is O, S, SO₂, or CH₂.
 38. The method of claim 37, wherein the compound has the structure of Formula V:

or a pharmaceutically acceptable salt or ester thereof; wherein: R¹, R², and R³ are each independently H, phosphate, monphosphate, diphosphate, triphosphate, a stabilized phosphate prodrug, acyl, lower acyl, alkyl, lower alkyl, or a pharmaceutically acceptable leaving group which, when administered in vivo, provides a compound wherein R¹, R², and R³ are each independently H or phosphate; Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵, or SR⁴; X¹ is selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵, and SR⁵; and each R⁴ and R⁵ is independently hydrogen, acyl, lower acyl, alkyl, or lower alkyl.
 39. The method of claim 38, wherein: R¹, R², and R³ are each independently H; phosphate; a stabilized phosphate prodrug; acyl; or a pharmaceutically acceptable leaving group which, when administered in vivo, provides a compound wherein R¹, R², and R³ are each independently H or phosphate; Y is hydrogen, bromo, chloro, fluoro, iodo, OR⁴, NR⁴R⁵, or SR⁴; X¹ is selected from the group consisting of H, straight chained, branched or cyclic alkyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, chloro, bromo, fluoro, iodo, OR⁴, NR⁴NR⁵, and SR⁵; and each R⁴ and R⁵ is independently hydrogen, acyl, or alkyl.
 40. The method of claim 37, wherein: Base is a pyrimidine base; R¹, R², and R³ are each independently H, phosphate, a stabilized phosphate prodrug, acyl, or a pharmaceutically acceptable leaving group which, when administered in vivo, provides a compound wherein R¹ and R² are each independently H or phosphate; R⁶ is hydroxy, alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, fluoro, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; R⁷ is hydrogen, OR³, hydroxyl, azido, cyano, alkynyl, halo, or NH₂; and X is O.
 41. The method of claim 37, wherein R¹ and R² are each independently H; phosphate; a stabilized phosphate prodrug; acyl; or a pharmaceutically acceptable leaving group which, when administered in vivo, provides a compound wherein R¹ and R² are each independently H or phosphate.
 42. The method of claim 37, wherein R¹ is hydrogen, acyl, or phosphate.
 43. The method of claim 37, wherein R¹ is hydrogen or phosphate.
 44. The method of claim 37, wherein R¹ is phosphate.
 45. The method of claim 37, wherein R² is hydrogen or acyl.
 46. The method of claim 37, wherein R² is hydrogen.
 47. The method of claim 37, wherein R⁶ is alkyl.
 48. The method of claim 37, wherein R⁶ is methyl.
 49. The method of claim 37, wherein R⁷ is hydrogen, OR², hydroxy, alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂.
 50. The method of claim 37, wherein R⁷ is hydrogen, OR², alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —O(alkenyl), chloro, bromo, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂.
 51. The method of claim 37, wherein R⁷ is hydrogen, OR², hydroxy, azido, cyano, alkynyl, chloro, bromo, iodo, or NH₂.
 52. The method of claim 37, wherein R⁷ is hydroxy.
 53. The method of claim 37, wherein R⁷ is azido.
 54. The method of claim 37, wherein R⁷ is cyano.
 55. The method of claim 37, wherein R⁷ is alkynyl.
 56. The method of claim 55, wherein R⁷ is ethynyl.
 57. The method of claim 37, wherein R⁷ is halo.
 58. The method of claim 37, wherein R⁷ is chloro, bromo, or iodo.
 59. The method of claim 37, wherein R⁷ is chloro.
 60. The method of claim 37, wherein R⁷ is NH₂.
 61. The method of claim 37, wherein X is O.
 62. The method of claim 37, wherein Base is selected from the group consisting of cytosinyl, 5-azacytocinyl, 6-azacytosinyl, 5-fluorocytosinyl, 5-methylcytosinyl, 6-azapyrimidinyl, 2-mercaptopyrmidinyl, 4-mercaptopyrmidinyl, C⁵-alkylpyrimidinyls, C⁵-benzylpyrimidinyls, C⁵-halopyrimidinyls, C⁵-vinylpyrimidinyl, C⁵-acetylenic pyrimidinyl, C⁵-acyl pyrimidinyl, C⁵-amidopyrimidinyl, C⁵-cyanopyrimidinyl, C⁵-nitropyrimidinyl, C⁵-aminopyrimidinyl, thyminyl, uracilyl, 5-halouracilyl, 5-fluorouracilyl, and 5-azauracilyl.
 63. The method of claim 37, wherein Base is cytosinyl, N-acetylcytosinyl, N,N-diacetyl)cytosinyl, N-methylcytosinyl, N-ethylcytosinyl, N-cyclopropylcytosinyl, thyminyl, 2,4-O-diacetylthyminyl, uracilyl, 5-fluorouracilyl, 4-O-acetyluracilyl, 2,4-O-diacetyluracilyl, 4-O-methyluracilyl, 4-O-ethyluracilyl, or 4-O-cyclopropyluracilyl.
 64. The method of claim 37, wherein Base is cytosinyl, thyminyl, or uracilyl.
 65. The method of claim 37, wherein Base is cytosinyl.
 66. The method of claim 37, wherein Base is thyminyl.
 67. The method of claim 37, wherein Base is uracilyl.
 68. The method of claim 37, wherein Base is selected from the group consisting of:


69. The method of claim 39, wherein Base is selected from the group consisting of:


70. The method of claim 37, wherein: Base is a pyrimidine base; R¹, R², and R³ are each independently H; phosphate; a stabilized phosphate prodrug; acyl; or a pharmaceutically acceptable leaving group which, when administered in vivo, provides a compound wherein R¹ and R² are each independently H or phosphate; R⁶ is alkyl; R⁷ is hydrogen, OR³, hydroxy, alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; and X is O.
 71. The method of claim 37, wherein: Base is a pyrimidine base; R¹ is hydrogen or phosphate; R² is hydrogen or acyl; R⁶ is alkyl; R⁷ is hydrogen, OR², hydroxy, azido, cyano, alkynyl, chloro, bromo, iodo, or NH₂; R¹⁰ is hydrogen; and X is O.
 72. The method of claim 1, comprising administering the compound or a pharmaceutically acceptable salt or ester thereof in combination or alternation with a second anti-hepatitis C virus agent.
 73. The method of claim 72, wherein the second anti-hepatitis C virus agent is selected from the group consisting of interferon, ribavirin, a protease inhibitor, a thiazolidine derivative, a polymerase inhibitor, and a helicase inhibitor.
 74. The method of claim 72, wherein the second anti-hepatitis C virus agent is interferon.
 75. The method of claim 72, wherein the second anti-hepatitis C virus agent is a protease inhibitor.
 76. The method of claim 72, wherein the second anti-hepatitis C virus agent is ribavirin.
 77. The method of claim 1, wherein the compound is in the form of a dosage unit.
 78. The method of claim 77, wherein the dosage unit contains from about 50 to about 1000 mg of the compound.
 79. The method of claim 77, wherein the dosage unit is a tablet or capsule.
 80. The method of claim 1, wherein the host is a human.
 81. The method of claim 1, wherein the compound is in substantially pure form.
 82. The method of claim 1, wherein the compound is at least 90% by weight of the 13-D-isomer.
 83. The method of claim 1, wherein the compound is at least 95% by weight of the 13-D-isomer.
 84. A method for inhibiting the replication of a hepatitis C virus in a host, comprising contacting the host with an anti-virally effective amount of a compound of Formula XVII:

or a pharmaceutically acceptable salt or ester thereof; wherein: Base is a pyrimidine base; R¹ and R² are each independently H, phosphate, monophosphate, diphosphate, triphosphoate, a stabilized phosphate prodrug, acyl, lower acyl, alkyl, lower alkyl, or a pharmaceutically acceptable leaving group which, when administered in vivo, provides a compound wherein R¹ and R² are each independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl, lower alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), halo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; R⁷ and R⁹ are each independently hydrogen, OR², hydroxy, alkyl, lower alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; R¹⁰ is H, alkyl, lower alkyl, or halo; alternatively, R⁷ and R⁹, or R⁷ and R¹⁰ can come together to form a bond; and X is O, S, SO₂, or CH₂.
 85. The method of claim 84, wherein the host is a cell.
 86. A method for inhibiting the replication of a hepatitis C virus in a host, comprising contacting the host with an anti-virally effective amount of a compound of Formula X or XI:

or a pharmaceutically acceptable salt or ester thereof; wherein: Base is a pyrimidine base; R¹, R², and R³ are each independently H, phosphate, monophosphate, diphosphate, triphosphoate, a stabilized phosphate prodrug, acyl, lower acyl, alkyl, lower alkyl, or a pharmaceutically acceptable leaving group which, when administered in vivo, provides a compound wherein R¹, R², and R³ are each independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl, lower alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), halo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; R⁷ is hydrogen, OR³, hydroxy, alkyl, lower alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), halo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; X is O, S, SO₂, or CH₂.
 87. The method of claim 86, wherein the host is a cell.
 88. A method for inhibiting the replication of a hepatitis C virus in a host, comprising contacting a polymerase of the host with an anti-virally effective amount of a compound of Formula XVII:

or a pharmaceutically acceptable salt or ester thereof; wherein: Base is a pyrimidine base; R¹ and R² are each independently H, phosphate, monophosphate, diphosphate, triphosphoate, a stabilized phosphate prodrug, acyl, lower acyl, alkyl, lower alkyl, or a pharmaceutically acceptable leaving group which, when administered in vivo, provides a compound wherein R¹ and R² are each independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl, lower alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), halo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; R⁷ and R⁹ are each independently hydrogen, OR², hydroxy, alkyl, lower alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), chloro, bromo, iodo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; R¹⁰ is H, alkyl, lower alkyl, or halo; alternatively, R⁷ and R⁹, or R⁷ and R¹⁰ can come together to form a bond; and X is O, S, SO₂, or CH₂.
 89. The method of claim 88, wherein the host is a cell.
 90. A method for inhibiting the replication of a hepatitis C virus in a host, comprising contacting a polymerase of the host with an anti-virally effective amount of a compound of Formula X or XI:

or a pharmaceutically acceptable salt or ester thereof; wherein: Base is a pyrimidine base; R¹, R², and R³ are each independently H, phosphate, monophosphate, diphosphate, triphosphoate, a stabilized phosphate prodrug, acyl, lower acyl, alkyl, lower alkyl, or a pharmaceutically acceptable leaving group which, when administered in vivo, provides a compound wherein R¹, R², and R³ are each independently H or phosphate; R⁶ is hydrogen, hydroxy, alkyl, lower alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), halo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; R⁷ is hydrogen, OR³, hydroxy, alkyl, lower alkyl, azido, cyano, alkenyl, alkynyl, Br-vinyl, —C(O)O(alkyl), —C(O)O(lower alkyl), —O(acyl), —O(lower acyl), —O(alkyl), —O(lower alkyl), —O(alkenyl), halo, NO₂, NH₂, —NH(lower alkyl), —NH(acyl), —N(lower alkyl)₂, or —N(acyl)₂; X is O, S, SO₂, or CH₂.
 91. The method of claim 90, wherein the host is a cell. 